| 156273542 | CV2320193 | single nucleotide variant | NM_144711.6(KLHL23):c.49A>G (p.Thr17Ala) | not specified [RCV004169816] | likely benign | 2 | 169735063 | 169735063 | Human | | name |
| 407481496 | CV3448541 | single nucleotide variant | NM_144711.6(KLHL23):c.70G>A (p.Asp24Asn) | not specified [RCV004644112] | uncertain significance | 2 | 169735084 | 169735084 | Human | | name |
| 156296388 | CV2310406 | single nucleotide variant | NM_144711.6(KLHL23):c.158C>T (p.Ala53Val) | not specified [RCV004163447] | uncertain significance | 2 | 169735172 | 169735172 | Human | | name |
| 405813344 | CV3265807 | single nucleotide variant | NM_144711.6(KLHL23):c.160G>A (p.Val54Ile) | not specified [RCV004409356] | uncertain significance | 2 | 169735174 | 169735174 | Human | | name |
| 597640069 | CV3692368 | single nucleotide variant | NM_144711.6(KLHL23):c.218A>C (p.Lys73Thr) | not specified [RCV004941464] | uncertain significance | 2 | 169735232 | 169735232 | Human | | name |
| 597640082 | CV3692370 | single nucleotide variant | NM_144711.6(KLHL23):c.189G>T (p.Lys63Asn) | not specified [RCV004941466] | uncertain significance | 2 | 169735203 | 169735203 | Human | | name |
| 156218321 | CV2253940 | single nucleotide variant | NM_144711.6(KLHL23):c.887C>T (p.Thr296Ile) | not specified [RCV004127615] | uncertain significance | 2 | 169735901 | 169735901 | Human | | name |
| 155929251 | CV2278032 | single nucleotide variant | NM_144711.6(KLHL23):c.991G>A (p.Asp331Asn) | not specified [RCV004141259] | uncertain significance | 2 | 169736005 | 169736005 | Human | | name |
| 155985283 | CV2345073 | single nucleotide variant | NM_144711.6(KLHL23):c.650A>G (p.Glu217Gly) | not specified [RCV004193351] | uncertain significance | 2 | 169735664 | 169735664 | Human | | name |
| 405813346 | CV3265808 | single nucleotide variant | NM_144711.6(KLHL23):c.556A>G (p.Ile186Val) | not specified [RCV004409357] | uncertain significance | 2 | 169735570 | 169735570 | Human | | name |
| 405813348 | CV3276122 | single nucleotide variant | NM_144711.6(KLHL23):c.727A>G (p.Arg243Gly) | not specified [RCV004409358] | uncertain significance | 2 | 169735741 | 169735741 | Human | | name |
| 405813350 | CV3276123 | single nucleotide variant | NM_144711.6(KLHL23):c.798G>T (p.Glu266Asp) | not specified [RCV004409359] | uncertain significance | 2 | 169735812 | 169735812 | Human | | name |
| 407481485 | CV3448539 | single nucleotide variant | NM_144711.6(KLHL23):c.647T>C (p.Ile216Thr) | not specified [RCV004644110] | uncertain significance | 2 | 169735661 | 169735661 | Human | | name |
| 407481500 | CV3448542 | single nucleotide variant | NM_144711.6(KLHL23):c.431C>G (p.Ser144Cys) | not specified [RCV004644113] | uncertain significance | 2 | 169735445 | 169735445 | Human | | name |
| 407481505 | CV3448544 | single nucleotide variant | NM_144711.6(KLHL23):c.881C>A (p.Pro294His) | not specified [RCV004644114] | uncertain significance | 2 | 169735895 | 169735895 | Human | | name |
| 597640062 | CV3692367 | single nucleotide variant | NM_144711.6(KLHL23):c.314G>T (p.Arg105Ile) | not specified [RCV004941463] | uncertain significance | 2 | 169735328 | 169735328 | Human | | name |
| 597640076 | CV3692369 | single nucleotide variant | NM_144711.6(KLHL23):c.588A>C (p.Lys196Asn) | not specified [RCV004941465] | uncertain significance | 2 | 169735602 | 169735602 | Human | | name |
| 598182787 | CV3987326 | single nucleotide variant | NM_144711.6(KLHL23):c.902A>G (p.Gln301Arg) | not specified [RCV005352791] | uncertain significance | 2 | 169735916 | 169735916 | Human | | name |
| 598161542 | CV3987327 | single nucleotide variant | NM_144711.6(KLHL23):c.301G>A (p.Glu101Lys) | not specified [RCV005368455] | uncertain significance | 2 | 169735315 | 169735315 | Human | | name |
| 598161547 | CV3987332 | single nucleotide variant | NM_144711.6(KLHL23):c.674A>G (p.Tyr225Cys) | not specified [RCV005368456] | uncertain significance | 2 | 169735688 | 169735688 | Human | | name |
| 15179995 | CV707845 | single nucleotide variant | NM_144711.6(KLHL23):c.791A>G (p.His264Arg) | not provided [RCV000974044] | benign | 2 | 169735805 | 169735805 | Human | | name |
| 156086243 | CV2390797 | single nucleotide variant | NM_144711.6(KLHL23):c.1673T>A (p.Val558Asp) | not specified [RCV004241080] | uncertain significance | 2 | 169749728 | 169749728 | Human | | name |
| 156263406 | CV2391699 | single nucleotide variant | NM_144711.6(KLHL23):c.1565C>T (p.Thr522Met) | not specified [RCV004241854] | uncertain significance | 2 | 169749620 | 169749620 | Human | | name |
| 329367371 | CV2427380 | single nucleotide variant | NM_144711.6(KLHL23):c.1457A>C (p.Asn486Thr) | not specified [RCV004248236] | uncertain significance | 2 | 169749512 | 169749512 | Human | | name |
| 401883500 | CV2757945 | single nucleotide variant | NM_144711.6(KLHL23):c.1195A>G (p.Ile399Val) | not specified [RCV004337079] | uncertain significance | 2 | 169736209 | 169736209 | Human | | name |
| 401868661 | CV2767302 | single nucleotide variant | NM_144711.6(KLHL23):c.1504G>A (p.Gly502Ser) | not specified [RCV004349470] | uncertain significance | 2 | 169749559 | 169749559 | Human | | name |
| 401862761 | CV2778997 | single nucleotide variant | NM_144711.6(KLHL23):c.1492A>G (p.Arg498Gly) | not specified [RCV004348651] | uncertain significance | 2 | 169749547 | 169749547 | Human | | name |
| 405813337 | CV3265804 | single nucleotide variant | NM_144711.6(KLHL23):c.1340G>A (p.Ser447Asn) | not specified [RCV004409353] | uncertain significance | 2 | 169741511 | 169741511 | Human | | name |
| 405813339 | CV3265805 | single nucleotide variant | NM_144711.6(KLHL23):c.1459G>C (p.Glu487Gln) | not specified [RCV004409354] | uncertain significance | 2 | 169749514 | 169749514 | Human | | name |
| 405813341 | CV3265806 | single nucleotide variant | NM_144711.6(KLHL23):c.1579A>G (p.Ile527Val) | not specified [RCV004409355] | uncertain significance | 2 | 169749634 | 169749634 | Human | | name |
| 407481490 | CV3448540 | single nucleotide variant | NM_144711.6(KLHL23):c.1405T>A (p.Tyr469Asn) | not specified [RCV004644111] | uncertain significance | 2 | 169749460 | 169749460 | Human | | name |
| 407481511 | CV3448545 | single nucleotide variant | NM_144711.6(KLHL23):c.1333G>A (p.Glu445Lys) | not specified [RCV004644115] | uncertain significance | 2 | 169741504 | 169741504 | Human | | name |
| 407481514 | CV3448546 | single nucleotide variant | NM_144711.6(KLHL23):c.1598A>G (p.Asp533Gly) | not specified [RCV004644116] | uncertain significance | 2 | 169749653 | 169749653 | Human | | name |
| 598221122 | CV3987330 | single nucleotide variant | NM_144711.6(KLHL23):c.1141G>A (p.Ala381Thr) | not specified [RCV005360763] | uncertain significance | 2 | 169736155 | 169736155 | Human | | name |
| 598221130 | CV3987331 | single nucleotide variant | NM_144711.6(KLHL23):c.1396A>C (p.Asn466His) | not specified [RCV005360764] | uncertain significance | 2 | 169749451 | 169749451 | Human | | name |
| 598182794 | CV3987333 | single nucleotide variant | NM_144711.6(KLHL23):c.1100T>G (p.Leu367Trp) | not specified [RCV005352792] | uncertain significance | 2 | 169736114 | 169736114 | Human | | name |
| 598221138 | CV3987334 | single nucleotide variant | NM_144711.6(KLHL23):c.1498G>A (p.Glu500Lys) | not specified [RCV005360765] | uncertain significance | 2 | 169749553 | 169749553 | Human | | name |