ClinVar Miner

List of variants in gene LARS2 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
Download table as spreadsheet
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.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.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.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.255C>T (p.Tyr85=) rs114881088 0.00157
NM_015340.4(LARS2):c.1008C>T (p.Val336=) rs142803778 0.00047
NM_015340.4(LARS2):c.1178C>A (p.Ala393Asp) rs138121304 0.00029
NM_015340.4(LARS2):c.944C>T (p.Ser315Leu) rs755162646 0.00004
NM_015340.4(LARS2):c.1197A>G (p.Glu399=) rs187209664 0.00002
NM_015340.4(LARS2):c.362A>G (p.Gln121Arg) rs200681375 0.00002
NM_015340.4(LARS2):c.1123+7A>T
NM_015340.4(LARS2):c.1240-7C>T
NM_015340.4(LARS2):c.1523+10_1523+20del
NM_015340.4(LARS2):c.1523+9_1523+10insAGTT
NM_015340.4(LARS2):c.1938C>T (p.Asn646=) rs138012553
NM_015340.4(LARS2):c.2412G>A (p.Ala804=)
NM_015340.4(LARS2):c.414C>T (p.Ala138=)
NM_015340.4(LARS2):c.945G>C (p.Ser315=) rs145135580

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.