ClinVar Miner

List of variants in gene LARS2 reported as benign for not specified

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Gene type:
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Total variants: 22
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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.945G>C (p.Ser315=) rs145135580

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