ClinVar Miner

List of variants in gene LARS2 studied for not specified

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Gene type:
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Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_015340.4(LARS2):c.2358A>G (p.Val786=) rs267220 0.87505
NM_015340.4(LARS2):c.2169T>C (p.Ala723=) rs2170549 0.85995
NM_015340.4(LARS2):c.1053T>C (p.Leu351=) rs7610357 0.78771
NM_015340.4(LARS2):c.1455G>A (p.Ala485=) rs2128361 0.78756
NM_015340.4(LARS2):c.1760+12T>C rs2306522 0.50630
NM_015340.4(LARS2):c.1983G>A (p.Thr661=) rs11549809 0.26851
NM_015340.4(LARS2):c.-36G>A rs75054661 0.03806
NM_015340.4(LARS2):c.972C>A (p.His324Gln) rs71645922 0.02237
NM_015340.4(LARS2):c.2181G>T (p.Lys727Asn) rs36054230 0.01430
NM_015340.4(LARS2):c.2493G>T (p.Glu831Asp) rs9827689 0.01205
NM_015340.4(LARS2):c.2124T>C (p.Ser708=) rs34459812 0.01189
NM_015340.4(LARS2):c.157T>C (p.Leu53=) rs141607519 0.00680
NM_015340.4(LARS2):c.22T>C (p.Leu8=) rs77377258 0.00549
NM_015340.4(LARS2):c.1131C>T (p.Pro377=) rs144183054 0.00518
NM_015340.4(LARS2):c.765G>A (p.Ala255=) rs116272561 0.00466
NM_015340.4(LARS2):c.1552G>A (p.Asp518Asn) rs116826217 0.00451
NM_015340.4(LARS2):c.2307C>T (p.Ser769=) rs143838895 0.00280
NM_015340.4(LARS2):c.2602G>A (p.Glu868Lys) rs34965084 0.00260
NM_015340.4(LARS2):c.2547T>C (p.Ala849=) rs78587006 0.00217
NM_015340.4(LARS2):c.1692C>T (p.Ala564=) rs149911756 0.00203
NM_015340.4(LARS2):c.235-12G>A rs75240042 0.00168
NM_015340.4(LARS2):c.255C>T (p.Tyr85=) rs114881088 0.00157
NM_015340.4(LARS2):c.1989G>T (p.Arg663=) rs139111439 0.00056
NM_015340.4(LARS2):c.2211T>C (p.Ser737=) rs371382425 0.00051
NM_015340.4(LARS2):c.1008C>T (p.Val336=) rs142803778 0.00047
NM_015340.4(LARS2):c.2203G>A (p.Val735Ile) rs141011840 0.00045
NM_015340.4(LARS2):c.1622+8G>A rs202009605 0.00030
NM_015340.4(LARS2):c.1178C>A (p.Ala393Asp) rs138121304 0.00029
NM_015340.4(LARS2):c.488G>A (p.Arg163His) rs150185028 0.00029
NM_015340.4(LARS2):c.338G>A (p.Arg113Gln) rs138437422 0.00023
NM_015340.4(LARS2):c.1947C>A (p.Asp649Glu) rs143155251 0.00022
NM_015340.4(LARS2):c.2620G>A (p.Glu874Lys) rs142215302 0.00015
NM_015340.4(LARS2):c.1383T>C (p.Ile461=) rs35347543 0.00014
NM_015340.4(LARS2):c.1861+7A>G rs369084897 0.00008
NM_015340.4(LARS2):c.1622+7C>T rs770655297 0.00006
NM_015340.4(LARS2):c.1782G>T (p.Leu594=) rs145796540 0.00006
NM_015340.4(LARS2):c.180G>C (p.Glu60Asp) rs199568924 0.00006
NM_015340.4(LARS2):c.1814G>A (p.Arg605His) rs142665087 0.00006
NM_015340.4(LARS2):c.763G>A (p.Ala255Thr) rs201911936 0.00006
NM_015340.4(LARS2):c.1104C>G (p.Gly368=) rs747618737 0.00004
NM_015340.4(LARS2):c.1123+8G>C rs770963717 0.00004
NM_015340.4(LARS2):c.2490G>A (p.Pro830=) rs374014256 0.00004
NM_015340.4(LARS2):c.2214+13C>G rs876657487 0.00003
NM_015340.4(LARS2):c.2278A>G (p.Ser760Gly) rs781382275 0.00002
NM_015340.4(LARS2):c.2404+4C>T rs199693918 0.00002
NM_015340.4(LARS2):c.2404+5G>A rs752860955 0.00002
NM_015340.4(LARS2):c.-103C>G rs1553625369 0.00001
NM_015340.4(LARS2):c.-21-13C>T rs779418705 0.00001
NM_015340.4(LARS2):c.-88+6C>A rs767039300 0.00001
NM_015340.4(LARS2):c.1124-8C>G rs1057523863 0.00001
NM_015340.4(LARS2):c.1452C>T (p.Ile484=) rs772146255 0.00001
NM_015340.4(LARS2):c.1840A>G (p.Arg614Gly) rs1447357435 0.00001
NM_015340.4(LARS2):c.219A>G (p.Lys73=) rs754475523 0.00001
NM_015340.4(LARS2):c.2572C>A (p.Gln858Lys) rs777893707 0.00001
NM_015340.4(LARS2):c.-88+10C>G rs1553625371
NM_015340.4(LARS2):c.1053T>A (p.Leu351=) rs7610357
NM_015340.4(LARS2):c.1530G>A (p.Lys510=) rs752585512
NM_015340.4(LARS2):c.1626T>C (p.Pro542=) rs1352189510
NM_015340.4(LARS2):c.1753A>G (p.Lys585Glu) rs1181180156
NM_015340.4(LARS2):c.1938C>T (p.Asn646=) rs138012553
NM_015340.4(LARS2):c.2044+14del rs1553637400
NM_015340.4(LARS2):c.2112G>A (p.Glu704=) rs876657486
NM_015340.4(LARS2):c.2169T>A (p.Ala723=) rs2170549
NM_015340.4(LARS2):c.2292+8G>T rs876657488
NM_015340.4(LARS2):c.2292+8_2292+9delinsTT rs1064795560
NM_015340.4(LARS2):c.235-19C>A rs1057524188
NM_015340.4(LARS2):c.363+13G>A rs944920117
NM_015340.4(LARS2):c.416C>T (p.Ala139Val) rs1553628118
NM_015340.4(LARS2):c.693A>G (p.Ala231=) rs779700014
NM_015340.4(LARS2):c.879C>T (p.Gly293=) rs368510008
NM_015340.4(LARS2):c.945G>A (p.Ser315=) rs145135580
NM_015340.4(LARS2):c.945G>C (p.Ser315=) rs145135580

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