| 156335520 | CV2272908 | single nucleotide variant | NM_017448.5(LDHC):c.7A>G (p.Thr3Ala) | not specified [RCV004135804] | uncertain significance | 11 | 18412724 | 18412724 | Human | | name |
| 155960068 | CV2194133 | single nucleotide variant | NM_017448.5(LDHC):c.38T>C (p.Ile13Thr) | not specified [RCV004076887] | uncertain significance | 11 | 18412755 | 18412755 | Human | | name |
| 401859728 | CV2771810 | single nucleotide variant | NM_017448.5(LDHC):c.60G>C (p.Gln20His) | not specified [RCV004350577] | uncertain significance | 11 | 18412777 | 18412777 | Human | | name |
| 597632560 | CV3698928 | single nucleotide variant | NM_017448.5(LDHC):c.55T>C (p.Ser19Pro) | not specified [RCV004940041] | uncertain significance | 11 | 18412772 | 18412772 | Human | | name |
| 15116925 | CV712753 | single nucleotide variant | NM_017448.5(LDHC):c.37A>C (p.Ile13Leu) | not provided [RCV000962117] | benign | 11 | 18412754 | 18412754 | Human | | name |
| 156052695 | CV2329040 | single nucleotide variant | NM_017448.5(LDHC):c.169A>G (p.Lys57Glu) | not specified [RCV004180320] | uncertain significance | 11 | 18415226 | 18415226 | Human | | name |
| 405817669 | CV3280114 | single nucleotide variant | NM_017448.5(LDHC):c.158T>C (p.Val53Ala) | not specified [RCV004412621] | uncertain significance | 11 | 18415215 | 18415215 | Human | | name |
| 405817668 | CV3280115 | single nucleotide variant | NM_017448.5(LDHC):c.260C>G (p.Ala87Gly) | not specified [RCV004412622] | uncertain significance | 11 | 18429752 | 18429752 | Human | | name |
| 597632567 | CV3698930 | single nucleotide variant | NM_017448.5(LDHC):c.109A>G (p.Ile37Val) | not specified [RCV004940043] | uncertain significance | 11 | 18412826 | 18412826 | Human | | name |
| 155920739 | CV2210873 | single nucleotide variant | NM_017448.5(LDHC):c.505C>T (p.Arg169Cys) | not specified [RCV004085958] | uncertain significance | 11 | 18434826 | 18434826 | Human | | name |
| 156241621 | CV2213964 | single nucleotide variant | NM_017448.5(LDHC):c.740A>G (p.Tyr247Cys) | not specified [RCV004083687] | uncertain significance | 11 | 18446239 | 18446239 | Human | | name |
| 155908273 | CV2302390 | single nucleotide variant | NM_017448.5(LDHC):c.836G>A (p.Gly279Glu) | not specified [RCV004161136] | uncertain significance | 11 | 18450964 | 18450964 | Human | | name |
| 156183084 | CV2327945 | single nucleotide variant | NM_017448.5(LDHC):c.481A>G (p.Ser161Gly) | not specified [RCV004179262] | uncertain significance | 11 | 18434802 | 18434802 | Human | | name |
| 156308465 | CV2369930 | single nucleotide variant | NM_017448.5(LDHC):c.350T>C (p.Met117Thr) | not specified [RCV004208396] | uncertain significance | 11 | 18429842 | 18429842 | Human | | name |
| 329354562 | CV2448414 | single nucleotide variant | NM_017448.5(LDHC):c.475A>G (p.Ile159Val) | not specified [RCV004256698] | uncertain significance | 11 | 18434796 | 18434796 | Human | | name |
| 401743326 | CV2674633 | single nucleotide variant | NM_017448.5(LDHC):c.467C>G (p.Thr156Ser) | not specified [RCV004293931] | uncertain significance | 11 | 18434788 | 18434788 | Human | | name |
| 401723109 | CV2674713 | single nucleotide variant | NM_017448.5(LDHC):c.527A>G (p.Glu176Gly) | not specified [RCV004294000] | uncertain significance | 11 | 18434848 | 18434848 | Human | | name |
| 401735909 | CV2689208 | single nucleotide variant | NM_017448.5(LDHC):c.581G>A (p.Gly194Asp) | not specified [RCV004306054] | uncertain significance | 11 | 18434902 | 18434902 | Human | | name |
| 401887275 | CV2771853 | single nucleotide variant | NM_017448.5(LDHC):c.348A>G (p.Ile116Met) | not specified [RCV004344572] | uncertain significance | 11 | 18429840 | 18429840 | Human | | name |
| 401898527 | CV2788016 | single nucleotide variant | NM_017448.5(LDHC):c.787A>G (p.Ile263Val) | not specified [RCV004358668] | uncertain significance | 11 | 18446286 | 18446286 | Human | | name |
| 405817667 | CV3280116 | single nucleotide variant | NM_017448.5(LDHC):c.658A>G (p.Thr220Ala) | not specified [RCV004412623] | uncertain significance | 11 | 18438593 | 18438593 | Human | | name |
| 405817666 | CV3280117 | single nucleotide variant | NM_017448.5(LDHC):c.659C>T (p.Thr220Met) | not specified [RCV004412624] | uncertain significance | 11 | 18438594 | 18438594 | Human | | name |
| 407491622 | CV3452609 | single nucleotide variant | NM_017448.5(LDHC):c.915A>T (p.Lys305Asn) | not specified [RCV004642270] | uncertain significance | 11 | 18451043 | 18451043 | Human | | name |
| 597632563 | CV3698929 | single nucleotide variant | NM_017448.5(LDHC):c.317G>A (p.Arg106His) | not specified [RCV004940042] | uncertain significance | 11 | 18429809 | 18429809 | Human | | name |
| 597632572 | CV3698931 | single nucleotide variant | NM_017448.5(LDHC):c.772G>T (p.Asp258Tyr) | not specified [RCV004940044] | uncertain significance | 11 | 18446271 | 18446271 | Human | | name |