ClinVar Miner

List of variants in gene LARS2 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_015340.4(LARS2):c.2203G>A (p.Val735Ile) rs141011840 0.00045
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.1813C>T (p.Arg605Cys) rs147745374 0.00019
NM_015340.4(LARS2):c.2257A>G (p.Ile753Val) rs138699045 0.00014
NM_015340.4(LARS2):c.1075G>A (p.Val359Ile) rs575202634 0.00007
NM_015340.4(LARS2):c.180G>C (p.Glu60Asp) rs199568924 0.00006
NM_015340.4(LARS2):c.944C>T (p.Ser315Leu) rs755162646 0.00004
NM_015340.4(LARS2):c.1556C>T (p.Thr519Met) rs141097216 0.00002
NM_015340.4(LARS2):c.2278A>G (p.Ser760Gly) rs781382275 0.00002
NM_015340.4(LARS2):c.145A>G (p.Lys49Glu) rs777694670 0.00001
NM_015340.4(LARS2):c.1514C>T (p.Ser505Phe) rs750659632 0.00001
NM_015340.4(LARS2):c.1663G>C (p.Asp555His) rs1209939319 0.00001
NM_015340.4(LARS2):c.2546C>G (p.Ala849Gly) rs200160782 0.00001
NM_015340.4(LARS2):c.2572C>A (p.Gln858Lys) rs777893707 0.00001
NM_015340.4(LARS2):c.668A>G (p.His223Arg) rs775913371 0.00001
NM_015340.4(LARS2):c.739G>A (p.Ala247Thr) rs142506388 0.00001
NM_015340.4(LARS2):c.863A>T (p.His288Leu) rs751784781 0.00001
NM_015340.4(LARS2):c.1017A>G (p.Lys339=)
NM_015340.4(LARS2):c.1058A>C (p.Gln353Pro) rs2125727383
NM_015340.4(LARS2):c.1136C>G (p.Thr379Ser)
NM_015340.4(LARS2):c.125G>A (p.Ser42Asn) rs2125671988
NM_015340.4(LARS2):c.1453_1455delinsACA (p.Ala485Thr)
NM_015340.4(LARS2):c.1475G>T (p.Gly492Val)
NM_015340.4(LARS2):c.1564A>G (p.Thr522Ala)
NM_015340.4(LARS2):c.1753A>G (p.Lys585Glu) rs1181180156
NM_015340.4(LARS2):c.1801G>A (p.Gly601Arg)
NM_015340.4(LARS2):c.2018A>G (p.Glu673Gly)
NM_015340.4(LARS2):c.2069G>C (p.Arg690Thr)
NM_015340.4(LARS2):c.2101C>G (p.Arg701Gly)
NM_015340.4(LARS2):c.2521A>G (p.Met841Val)
NM_015340.4(LARS2):c.2536A>G (p.Asn846Asp)
NM_015340.4(LARS2):c.2560C>A (p.Pro854Thr) rs755182456
NM_015340.4(LARS2):c.359T>C (p.Met120Thr)
NM_015340.4(LARS2):c.424A>G (p.Arg142Gly) rs1403808001
NM_015340.4(LARS2):c.529T>A (p.Cys177Ser) rs1322452155
NM_015340.4(LARS2):c.788A>T (p.Tyr263Phe) rs1435320881
NM_015340.4(LARS2):c.800G>A (p.Gly267Asp)

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.