| 10407746 | CV213785 | single nucleotide variant | NM_015441.3(OLFML2B):c.44T>G (p.Val15Gly) | not provided [RCV000201108] | likely pathogenic | 1 | 162023387 | 162023387 | Human | | name |
| 405750934 | CV3370477 | single nucleotide variant | NM_015441.3(OLFML2B):c.34G>A (p.Ala12Thr) | not specified [RCV004499142] | uncertain significance | 1 | 162023397 | 162023397 | Human | | name |
| 405750964 | CV3370482 | single nucleotide variant | NM_015441.3(OLFML2B):c.95C>T (p.Pro32Leu) | not specified [RCV004499147] | uncertain significance | 1 | 162023336 | 162023336 | Human | | name |
| 155918768 | CV2333066 | single nucleotide variant | NM_015441.3(OLFML2B):c.257G>A (p.Arg86Gln) | not specified [RCV004194361] | uncertain significance | 1 | 162020100 | 162020100 | Human | | name |
| 155961883 | CV2388140 | single nucleotide variant | NM_015441.3(OLFML2B):c.170C>T (p.Ser57Phe) | not specified [RCV004241256] | uncertain significance | 1 | 162023261 | 162023261 | Human | | name |
| 329391450 | CV2448567 | single nucleotide variant | NM_015441.3(OLFML2B):c.286G>A (p.Ala96Thr) | not specified [RCV004259246] | likely benign | 1 | 162020071 | 162020071 | Human | | name |
| 401783628 | CV2723781 | single nucleotide variant | NM_015441.3(OLFML2B):c.247C>A (p.Pro83Thr) | not specified [RCV004325938] | uncertain significance | 1 | 162020110 | 162020110 | Human | | name |
| 407505532 | CV3469772 | single nucleotide variant | NM_015441.3(OLFML2B):c.116C>T (p.Pro39Leu) | not specified [RCV004646148] | uncertain significance | 1 | 162023315 | 162023315 | Human | | name |
| 597734375 | CV3573798 | single nucleotide variant | NM_015441.3(OLFML2B):c.211G>C (p.Glu71Gln) | not specified [RCV004843246] | uncertain significance | 1 | 162020146 | 162020146 | Human | | name |
| 597660381 | CV3573805 | single nucleotide variant | NM_015441.3(OLFML2B):c.218C>T (p.Ser73Leu) | not specified [RCV004834945] | uncertain significance | 1 | 162020139 | 162020139 | Human | | name |
| 15195021 | CV696224 | single nucleotide variant | NM_015441.3(OLFML2B):c.1047T>C (p.Pro349=) | not provided [RCV000955806] | benign | 1 | 161998252 | 161998252 | Human | | name |
| 15112546 | CV706815 | single nucleotide variant | NM_015441.3(OLFML2B):c.1788T>C (p.Ala596=) | not provided [RCV000961318] | benign | 1 | 161984140 | 161984140 | Human | | name |
| 15183412 | CV706816 | single nucleotide variant | NM_015441.3(OLFML2B):c.1017C>T (p.Asn339=) | not provided [RCV000974868] | benign | 1 | 161998282 | 161998282 | Human | | name |
| 156399786 | CV2202222 | single nucleotide variant | NM_015441.3(OLFML2B):c.916G>T (p.Val306Phe) | not specified [RCV004078167] | uncertain significance | 1 | 162000146 | 162000146 | Human | | name |
| 156322948 | CV2205300 | single nucleotide variant | NM_015441.3(OLFML2B):c.577G>A (p.Glu193Lys) | not specified [RCV004079918] | uncertain significance | 1 | 162006443 | 162006443 | Human | | name |
| 156236824 | CV2206715 | single nucleotide variant | NM_015441.3(OLFML2B):c.889C>T (p.Arg297Trp) | not specified [RCV004083407] | uncertain significance | 1 | 162000173 | 162000173 | Human | | name |
| 156196757 | CV2259206 | single nucleotide variant | NM_015441.3(OLFML2B):c.626G>A (p.Arg209Gln) | not specified [RCV004122231] | uncertain significance | 1 | 162006394 | 162006394 | Human | | name |
| 156177578 | CV2355866 | single nucleotide variant | NM_015441.3(OLFML2B):c.862C>G (p.Arg288Gly) | not specified [RCV004201258] | uncertain significance | 1 | 162000200 | 162000200 | Human | | name |
| 156063181 | CV2380460 | single nucleotide variant | NM_015441.3(OLFML2B):c.557A>T (p.Lys186Ile) | not specified [RCV004218058] | uncertain significance | 1 | 162006463 | 162006463 | Human | | name |
| 329367970 | CV2442599 | single nucleotide variant | NM_015441.3(OLFML2B):c.539T>C (p.Leu180Pro) | not specified [RCV004264958] | uncertain significance | 1 | 162017407 | 162017407 | Human | | name |
| 329352829 | CV2470576 | single nucleotide variant | NM_015441.3(OLFML2B):c.302A>C (p.Asp101Ala) | not specified [RCV004273578] | uncertain significance | 1 | 162020055 | 162020055 | Human | | name |
| 401730606 | CV2689752 | single nucleotide variant | NM_015441.3(OLFML2B):c.368C>T (p.Ser123Leu) | not specified [RCV004297663] | uncertain significance | 1 | 162019989 | 162019989 | Human | | name |
| 401746824 | CV2731979 | single nucleotide variant | NM_015441.3(OLFML2B):c.527G>A (p.Arg176Gln) | not specified [RCV004333214] | uncertain significance | 1 | 162017419 | 162017419 | Human | | name |
| 401890412 | CV2778689 | single nucleotide variant | NM_015441.3(OLFML2B):c.677G>A (p.Arg226His) | not specified [RCV004346606] | uncertain significance | 1 | 162006343 | 162006343 | Human | | name |
| 401885559 | CV2783332 | single nucleotide variant | NM_015441.3(OLFML2B):c.661A>G (p.Ser221Gly) | not specified [RCV004365697] | uncertain significance | 1 | 162006359 | 162006359 | Human | | name |
| 401880599 | CV2792904 | single nucleotide variant | NM_015441.3(OLFML2B):c.829C>T (p.Arg277Trp) | not specified [RCV004365640] | uncertain significance | 1 | 162000233 | 162000233 | Human | | name |
| 405750940 | CV3370478 | single nucleotide variant | NM_015441.3(OLFML2B):c.730G>C (p.Glu244Gln) | not specified [RCV004499143] | uncertain significance | 1 | 162000332 | 162000332 | Human | | name |
| 405750951 | CV3370480 | single nucleotide variant | NM_015441.3(OLFML2B):c.754G>A (p.Val252Met) | not specified [RCV004499145] | uncertain significance | 1 | 162000308 | 162000308 | Human | | name |
| 405750956 | CV3370481 | single nucleotide variant | NM_015441.3(OLFML2B):c.775A>G (p.Ile259Val) | not specified [RCV004499146] | uncertain significance | 1 | 162000287 | 162000287 | Human | | name |
| 407527323 | CV3469769 | single nucleotide variant | NM_015441.3(OLFML2B):c.400C>T (p.Leu134Phe) | not specified [RCV004655166] | uncertain significance | 1 | 162019957 | 162019957 | Human | | name |
| 597734369 | CV3573799 | single nucleotide variant | NM_015441.3(OLFML2B):c.808C>G (p.Pro270Ala) | not specified [RCV004843247] | uncertain significance | 1 | 162000254 | 162000254 | Human | | name |
| 597733896 | CV3573802 | single nucleotide variant | NM_015441.3(OLFML2B):c.432C>G (p.Asp144Glu) | not specified [RCV004843250] | uncertain significance | 1 | 162019925 | 162019925 | Human | | name |
| 597660373 | CV3573803 | single nucleotide variant | NM_015441.3(OLFML2B):c.335C>T (p.Ser112Leu) | not specified [RCV004834944] | uncertain significance | 1 | 162020022 | 162020022 | Human | | name |
| 597733801 | CV3573807 | single nucleotide variant | NM_015441.3(OLFML2B):c.430G>T (p.Asp144Tyr) | not specified [RCV004843252] | uncertain significance | 1 | 162019927 | 162019927 | Human | | name |
| 598182268 | CV3998494 | single nucleotide variant | NM_015441.3(OLFML2B):c.562C>T (p.Leu188Phe) | not specified [RCV005395110] | uncertain significance | 1 | 162006458 | 162006458 | Human | | name |
| 598161496 | CV3998496 | single nucleotide variant | NM_015441.3(OLFML2B):c.838C>A (p.Gln280Lys) | not specified [RCV005390632] | uncertain significance | 1 | 162000224 | 162000224 | Human | | name |
| 10407748 | CV213778 | single nucleotide variant | NM_015441.3(OLFML2B):c.2021G>A (p.Gly674Asp) | not provided [RCV000201143] | likely pathogenic | 1 | 161983907 | 161983907 | Human | | name |
| 10407751 | CV213779 | single nucleotide variant | NM_015441.3(OLFML2B):c.1606G>A (p.Gly536Ser) | not provided [RCV000201204] | likely pathogenic | 1 | 161984849 | 161984849 | Human | | name |
| 10407744 | CV213780 | single nucleotide variant | NM_015441.3(OLFML2B):c.1580G>A (p.Arg527Gln) | not provided [RCV000201057]|not specified [RCV004020482] | likely pathogenic|uncertain significance | 1 | 161984875 | 161984875 | Human | | name |
| 10407749 | CV213781 | single nucleotide variant | NM_015441.3(OLFML2B):c.1544G>A (p.Gly515Glu) | not provided [RCV000201186]|not specified [RCV004020481] | likely pathogenic|uncertain significance | 1 | 161984911 | 161984911 | Human | | name |
| 10407747 | CV213782 | single nucleotide variant | NM_015441.3(OLFML2B):c.1306G>T (p.Ala436Ser) | not provided [RCV000201124] | likely pathogenic | 1 | 161997993 | 161997993 | Human | | name |
| 10407745 | CV213783 | single nucleotide variant | NM_015441.3(OLFML2B):c.1058G>A (p.Arg353His) | not provided [RCV000201067]|not specified [RCV004020480] | likely pathogenic|likely benign | 1 | 161998241 | 161998241 | Human | | name |
| 10407750 | CV213784 | single nucleotide variant | NM_015441.3(OLFML2B):c.1039C>T (p.Arg347Trp) | not provided [RCV000201193] | likely pathogenic | 1 | 161998260 | 161998260 | Human | | name |
| 156281997 | CV2220687 | single nucleotide variant | NM_015441.3(OLFML2B):c.2143G>A (p.Glu715Lys) | not specified [RCV004097861] | uncertain significance | 1 | 161983785 | 161983785 | Human | | name |
| 155986192 | CV2233966 | single nucleotide variant | NM_015441.3(OLFML2B):c.1973C>T (p.Thr658Ile) | not specified [RCV004104308] | uncertain significance | 1 | 161983955 | 161983955 | Human | | name |
| 156132225 | CV2235303 | single nucleotide variant | NM_015441.3(OLFML2B):c.1265C>T (p.Ala422Val) | not specified [RCV004107337] | uncertain significance | 1 | 161998034 | 161998034 | Human | | name |
| 156269454 | CV2240137 | single nucleotide variant | NM_015441.3(OLFML2B):c.1475G>A (p.Gly492Glu) | not specified [RCV004110899] | uncertain significance | 1 | 161984980 | 161984980 | Human | | name |
| 156274057 | CV2279659 | single nucleotide variant | NM_015441.3(OLFML2B):c.1291G>A (p.Ala431Thr) | not specified [RCV004144286] | uncertain significance | 1 | 161998008 | 161998008 | Human | | name |
| 155927881 | CV2285272 | single nucleotide variant | NM_015441.3(OLFML2B):c.1588G>T (p.Val530Leu) | not specified [RCV004145464] | uncertain significance | 1 | 161984867 | 161984867 | Human | | name |
| 156275955 | CV2287674 | single nucleotide variant | NM_015441.3(OLFML2B):c.1751A>G (p.Asn584Ser) | not specified [RCV004141101] | uncertain significance | 1 | 161984177 | 161984177 | Human | | name |
| 156072035 | CV2353307 | single nucleotide variant | NM_015441.3(OLFML2B):c.1382C>T (p.Ser461Leu) | not specified [RCV004205776] | uncertain significance | 1 | 161997917 | 161997917 | Human | | name |
| 155903657 | CV2353636 | single nucleotide variant | NM_015441.3(OLFML2B):c.1087G>A (p.Asp363Asn) | not specified [RCV004199608] | uncertain significance | 1 | 161998212 | 161998212 | Human | | name |
| 155904496 | CV2353888 | single nucleotide variant | NM_015441.3(OLFML2B):c.1910A>G (p.Asp637Gly) | not specified [RCV004201886] | uncertain significance | 1 | 161984018 | 161984018 | Human | | name |
| 155990772 | CV2374806 | single nucleotide variant | NM_015441.3(OLFML2B):c.1471A>G (p.Ile491Val) | not specified [RCV004225407] | uncertain significance | 1 | 161997828 | 161997828 | Human | | name |
| 329370752 | CV2435675 | single nucleotide variant | NM_015441.3(OLFML2B):c.1960G>A (p.Ala654Thr) | not specified [RCV004254913] | uncertain significance | 1 | 161983968 | 161983968 | Human | | name |
| 329388441 | CV2471931 | single nucleotide variant | NM_015441.3(OLFML2B):c.1014C>G (p.His338Gln) | not specified [RCV004280949] | uncertain significance | 1 | 161998285 | 161998285 | Human | | name |
| 329393708 | CV2472101 | single nucleotide variant | NM_015441.3(OLFML2B):c.1286C>T (p.Pro429Leu) | not specified [RCV004283237] | uncertain significance | 1 | 161998013 | 161998013 | Human | | name |
| 401739170 | CV2722073 | single nucleotide variant | NM_015441.3(OLFML2B):c.2030T>G (p.Phe677Cys) | not specified [RCV004326551] | uncertain significance | 1 | 161983898 | 161983898 | Human | | name |
| 401888681 | CV2758047 | single nucleotide variant | NM_015441.3(OLFML2B):c.1702C>T (p.His568Tyr) | not specified [RCV004339213] | uncertain significance | 1 | 161984226 | 161984226 | Human | | name |
| 401884076 | CV2765959 | single nucleotide variant | NM_015441.3(OLFML2B):c.1738G>T (p.Ala580Ser) | not specified [RCV004337983] | uncertain significance | 1 | 161984190 | 161984190 | Human | | name |
| 401933123 | CV2806126 | single nucleotide variant | NM_015441.3(OLFML2B):c.1669T>C (p.Tyr557His) | not provided [RCV003409212] | uncertain significance | 1 | 161984259 | 161984259 | Human | | name |
| 405750863 | CV3370467 | single nucleotide variant | NM_015441.3(OLFML2B):c.1196C>T (p.Ser399Leu) | not specified [RCV004499132] | uncertain significance | 1 | 161998103 | 161998103 | Human | | name |
| 405750870 | CV3370468 | single nucleotide variant | NM_015441.3(OLFML2B):c.1358C>T (p.Pro453Leu) | not specified [RCV004499133] | uncertain significance | 1 | 161997941 | 161997941 | Human | | name |
| 405750879 | CV3370469 | single nucleotide variant | NM_015441.3(OLFML2B):c.1369G>C (p.Val457Leu) | not specified [RCV004499134] | uncertain significance | 1 | 161997930 | 161997930 | Human | | name |
| 405750882 | CV3370470 | single nucleotide variant | NM_015441.3(OLFML2B):c.1378G>C (p.Asp460His) | not specified [RCV004499135] | uncertain significance | 1 | 161997921 | 161997921 | Human | | name |
| 405750889 | CV3370471 | single nucleotide variant | NM_015441.3(OLFML2B):c.1412G>T (p.Gly471Val) | not specified [RCV004499136] | uncertain significance | 1 | 161997887 | 161997887 | Human | | name |
| 405750895 | CV3370472 | single nucleotide variant | NM_015441.3(OLFML2B):c.1463G>A (p.Arg488Gln) | not specified [RCV004499137] | uncertain significance | 1 | 161997836 | 161997836 | Human | | name |
| 405750903 | CV3370473 | single nucleotide variant | NM_015441.3(OLFML2B):c.1994G>A (p.Arg665His) | not specified [RCV004499138] | uncertain significance | 1 | 161983934 | 161983934 | Human | | name |
| 405750911 | CV3370474 | single nucleotide variant | NM_015441.3(OLFML2B):c.2006G>A (p.Arg669Gln) | not specified [RCV004499139] | uncertain significance | 1 | 161983922 | 161983922 | Human | | name |
| 405750917 | CV3370475 | single nucleotide variant | NM_015441.3(OLFML2B):c.2234A>T (p.His745Leu) | not specified [RCV004499140] | uncertain significance | 1 | 161983694 | 161983694 | Human | | name |
| 407527316 | CV3469766 | single nucleotide variant | NM_015441.3(OLFML2B):c.1612A>G (p.Thr538Ala) | not specified [RCV004655164] | uncertain significance | 1 | 161984843 | 161984843 | Human | | name |
| 407505526 | CV3469767 | single nucleotide variant | NM_015441.3(OLFML2B):c.1912G>A (p.Asp638Asn) | not specified [RCV004646146] | uncertain significance | 1 | 161984016 | 161984016 | Human | | name |
| 407527320 | CV3469768 | single nucleotide variant | NM_015441.3(OLFML2B):c.1505C>T (p.Thr502Met) | not specified [RCV004655165] | uncertain significance | 1 | 161984950 | 161984950 | Human | | name |
| 407527325 | CV3469770 | single nucleotide variant | NM_015441.3(OLFML2B):c.2165C>A (p.Thr722Asn) | not specified [RCV004655167] | uncertain significance | 1 | 161983763 | 161983763 | Human | | name |
| 407505529 | CV3469771 | single nucleotide variant | NM_015441.3(OLFML2B):c.1571A>T (p.Lys524Met) | not specified [RCV004646147] | uncertain significance | 1 | 161984884 | 161984884 | Human | | name |
| 597660366 | CV3573797 | single nucleotide variant | NM_015441.3(OLFML2B):c.1058G>T (p.Arg353Leu) | not specified [RCV004834943] | uncertain significance | 1 | 161998241 | 161998241 | Human | | name |
| 597734192 | CV3573800 | single nucleotide variant | NM_015441.3(OLFML2B):c.2020G>A (p.Gly674Ser) | not specified [RCV004843248] | uncertain significance | 1 | 161983908 | 161983908 | Human | | name |
| 597734038 | CV3573801 | single nucleotide variant | NM_015441.3(OLFML2B):c.1219G>A (p.Glu407Lys) | not specified [RCV004843249] | uncertain significance | 1 | 161998080 | 161998080 | Human | | name |
| 597733795 | CV3573804 | single nucleotide variant | NM_015441.3(OLFML2B):c.1781A>G (p.Tyr594Cys) | not specified [RCV004843251] | uncertain significance | 1 | 161984147 | 161984147 | Human | | name |
| 597660388 | CV3573808 | single nucleotide variant | NM_015441.3(OLFML2B):c.2159A>G (p.Tyr720Cys) | not specified [RCV004834946] | uncertain significance | 1 | 161983769 | 161983769 | Human | | name |
| 598161491 | CV3998495 | single nucleotide variant | NM_015441.3(OLFML2B):c.1784T>C (p.Val595Ala) | not specified [RCV005390631] | uncertain significance | 1 | 161984144 | 161984144 | Human | | name |
| 8624779 | CV79893 | single nucleotide variant | NM_015441.2(OLFML2B):c.1259C>T (p.Thr420Ile) | Malignant melanoma [RCV000059969] | not provided | 1 | 161998040 | 161998040 | Human | | name |
