ClinVar Miner

List of variants in gene LPIN2 reported as uncertain significance by GeneDx

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001375808.2(LPIN2):c.2671G>A (p.Asp891Asn) rs200648652 0.00033
NM_001375808.2(LPIN2):c.1781C>T (p.Pro594Leu) rs139826951 0.00026
NM_001375808.2(LPIN2):c.1132C>T (p.Pro378Ser) rs201678207 0.00018
NM_001375808.2(LPIN2):c.1489G>A (p.Glu497Lys) rs201325845 0.00013
NM_001375808.2(LPIN2):c.1514T>C (p.Ile505Thr) rs146424724 0.00013
NM_001375808.2(LPIN2):c.1339G>A (p.Val447Met) rs373758040 0.00007
NM_001375808.2(LPIN2):c.2399C>T (p.Pro800Leu) rs748431474 0.00006
NM_001375808.2(LPIN2):c.1099G>A (p.Ala367Thr) rs540544894 0.00005
NM_001375808.2(LPIN2):c.2650C>T (p.Arg884Ter) rs547662448 0.00005
NM_001375808.2(LPIN2):c.1375C>G (p.Leu459Val) rs781705610 0.00004
NM_001375808.2(LPIN2):c.1796C>T (p.Pro599Leu) rs372850864 0.00004
NM_001375808.2(LPIN2):c.2381T>C (p.Ile794Thr) rs183821298 0.00004
NM_001375808.2(LPIN2):c.56A>G (p.Tyr19Cys) rs371299772 0.00004
NM_001375808.2(LPIN2):c.959C>T (p.Thr320Ile) rs150648432 0.00004
NM_001375808.2(LPIN2):c.1274C>T (p.Ser425Leu) rs772737665 0.00003
NM_001375808.2(LPIN2):c.1115C>T (p.Ala372Val) rs201830346 0.00002
NM_001375808.2(LPIN2):c.1118C>T (p.Pro373Leu) rs772230305 0.00002
NM_001375808.2(LPIN2):c.1154C>T (p.Pro385Leu) rs754221410 0.00002
NM_001375808.2(LPIN2):c.1247C>T (p.Ala416Val) rs777239535 0.00002
NM_001375808.2(LPIN2):c.1348G>A (p.Ala450Thr) rs771486222 0.00002
NM_001375808.2(LPIN2):c.1814C>T (p.Ser605Leu) rs781778980 0.00002
NM_001375808.2(LPIN2):c.1144G>A (p.Val382Ile) rs1486044509 0.00001
NM_001375808.2(LPIN2):c.1492T>C (p.Phe498Leu) rs876660986 0.00001
NM_001375808.2(LPIN2):c.1631A>G (p.Glu544Gly) rs760055156 0.00001
NM_001375808.2(LPIN2):c.1720T>A (p.Ser574Thr) rs148779863 0.00001
NM_001375808.2(LPIN2):c.1745C>T (p.Pro582Leu) rs755110304 0.00001
NM_001375808.2(LPIN2):c.2171A>G (p.Asn724Ser) rs140915714 0.00001
NM_001375808.2(LPIN2):c.2617C>A (p.Pro873Thr) rs757315664 0.00001
NM_001375808.2(LPIN2):c.781C>G (p.His261Asp) rs876660984 0.00001
NM_001375808.2(LPIN2):c.1456+5G>T rs767379049
NM_001375808.2(LPIN2):c.1465A>C (p.Met489Leu) rs876660985
NM_001375808.2(LPIN2):c.2409G>C (p.Gln803His) rs876660987
NM_001375808.2(LPIN2):c.289G>A (p.Glu97Lys) rs2077534512
NM_001375808.2(LPIN2):c.560C>T (p.Ser187Phe) rs876660983

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