ClinVar Miner

List of variants in gene LARS2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_015340.4(LARS2):c.-22+127C>G rs78674974 0.04323
NM_015340.4(LARS2):c.2293-50G>A rs76190197 0.03506
NM_015340.4(LARS2):c.1239+34A>G rs116642917 0.01478
NM_015340.4(LARS2):c.1523+93G>C rs114869671 0.01475
NM_015340.4(LARS2):c.1623-176T>A rs146415564 0.01474
NM_015340.4(LARS2):c.1861+193C>A rs114889092 0.01473
NM_015340.4(LARS2):c.2292+98C>T rs115300907 0.01462
NM_015340.4(LARS2):c.2292+206C>T rs114332803 0.01461
NM_015340.4(LARS2):c.2404+173G>T rs41289598 0.01444
NM_015340.4(LARS2):c.1124-195C>G rs115000040 0.01183
NM_015340.4(LARS2):c.1760+234T>C rs148864127 0.01134
NM_015340.4(LARS2):c.-21-243T>C rs114795216 0.00954
NM_015340.4(LARS2):c.2044+284G>C rs115361910 0.00907
NM_015340.4(LARS2):c.235-340T>G rs147090571 0.00842
NM_015340.4(LARS2):c.1019-218T>A rs77944127 0.00622
NM_015340.4(LARS2):c.2215-136T>G rs114641494 0.00599
NM_015340.4(LARS2):c.765G>A (p.Ala255=) rs116272561 0.00466
NM_015340.4(LARS2):c.234+46A>G rs41289596 0.00396
NM_015340.4(LARS2):c.607-291G>A rs184412155 0.00366
NM_015340.4(LARS2):c.1124-32G>A rs139635763 0.00338
NM_015340.4(LARS2):c.606+196A>G rs376219315 0.00322
NM_015340.4(LARS2):c.517-221C>T rs368452663 0.00318
NM_015340.4(LARS2):c.1239+161T>C rs149850920 0.00315
NM_015340.4(LARS2):c.750+308G>T rs546073688 0.00306
NM_015340.4(LARS2):c.2533-85C>G rs577038160 0.00283
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.1239+51A>G rs139705937 0.00242
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.324C>T (p.Ser108=) rs140105027 0.00064
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.1622+8G>A rs202009605 0.00030
NM_015340.4(LARS2):c.1178C>A (p.Ala393Asp) rs138121304 0.00029
NM_015340.4(LARS2):c.1779G>C (p.Leu593=) rs148167639 0.00018
NM_015340.4(LARS2):c.235-7T>G rs200577813 0.00015
NM_015340.4(LARS2):c.1383T>C (p.Ile461=) rs35347543 0.00014
NM_015340.4(LARS2):c.1392C>T (p.Cys464=) rs775041032 0.00014
NM_015340.4(LARS2):c.2045-36C>T rs557280191 0.00009
NM_015340.4(LARS2):c.1622+7C>T rs770655297 0.00006
NM_015340.4(LARS2):c.2421G>A (p.Pro807=) rs777901333 0.00006
NM_015340.4(LARS2):c.2676G>A (p.Pro892=) rs550066510 0.00006
NM_015340.4(LARS2):c.517-4G>A rs756497084 0.00004
NM_015340.4(LARS2):c.1862-12T>C rs972686689 0.00003
NM_015340.4(LARS2):c.1197A>G (p.Glu399=) rs187209664 0.00002
NM_015340.4(LARS2):c.1557G>A (p.Thr519=) rs751609685 0.00002
NM_015340.4(LARS2):c.2238C>T (p.Asp746=) rs758417403 0.00002
NM_015340.4(LARS2):c.2404+4C>T rs199693918 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.1123+11A>G rs773989479 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.1866C>T (p.Ser622=) rs765622164 0.00001
NM_015340.4(LARS2):c.219A>G (p.Lys73=) rs754475523 0.00001
NM_015340.4(LARS2):c.2709T>C (p.Asp903=) rs772312219 0.00001
NM_015340.4(LARS2):c.*252C>T rs78404793
NM_015340.4(LARS2):c.-87-100C>A rs967355397
NM_015340.4(LARS2):c.-88+10C>G rs1553625371
NM_015340.4(LARS2):c.1053T>A (p.Leu351=) rs7610357
NM_015340.4(LARS2):c.1240-288G>A rs77373076
NM_015340.4(LARS2):c.1296G>A (p.Gly432=) rs866626104
NM_015340.4(LARS2):c.1302A>G (p.Arg434=) rs774454500
NM_015340.4(LARS2):c.1380C>T (p.Pro460=) rs1575289449
NM_015340.4(LARS2):c.1938C>T (p.Asn646=) rs138012553
NM_015340.4(LARS2):c.1974G>T (p.Gly658=) rs189078355
NM_015340.4(LARS2):c.2044+14del rs1553637400
NM_015340.4(LARS2):c.2169T>A (p.Ala723=) rs2170549
NM_015340.4(LARS2):c.2215-78dup rs564158098
NM_015340.4(LARS2):c.2292+8_2292+9delinsTT rs1064795560
NM_015340.4(LARS2):c.235-19C>A rs1057524188
NM_015340.4(LARS2):c.235-269del rs201088871
NM_015340.4(LARS2):c.2405-24C>A rs34191038
NM_015340.4(LARS2):c.363+13G>A rs944920117
NM_015340.4(LARS2):c.607-45dup rs749222943
NM_015340.4(LARS2):c.693A>G (p.Ala231=) rs779700014
NM_015340.4(LARS2):c.945G>A (p.Ser315=) rs145135580

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