ClinVar Miner

List of variants in gene LPIN2 studied for not specified

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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001375808.2(LPIN2):c.1169-88C>G rs3765622 0.31331
NM_001375808.2(LPIN2):c.1168+44T>C rs3826637 0.31167
NM_001375808.2(LPIN2):c.2442+87A>G rs2282635 0.30203
NM_001375808.2(LPIN2):c.*3C>T rs3745012 0.26634
NM_001375808.2(LPIN2):c.-10+1342C>G rs59096963 0.03286
NM_001375808.2(LPIN2):c.-10+1343C>G rs58940048 0.03285
NM_001375808.2(LPIN2):c.2223C>T (p.Ala741=) rs17555442 0.01175
NM_001375808.2(LPIN2):c.1867C>T (p.Pro623Ser) rs143090653 0.00873
NM_001375808.2(LPIN2):c.1801G>A (p.Glu601Lys) rs61735393 0.00824
NM_001375808.2(LPIN2):c.147C>T (p.His49=) rs17886056 0.00707
NM_001375808.2(LPIN2):c.1510C>T (p.Leu504Phe) rs104895500 0.00253
NM_001375808.2(LPIN2):c.120T>C (p.Asp40=) rs143261167 0.00243
NM_001375808.2(LPIN2):c.2327+11G>A rs148930095 0.00240
NM_001375808.2(LPIN2):c.1410C>T (p.Thr470=) rs35932462 0.00159
NM_001375808.2(LPIN2):c.1159A>G (p.Lys387Glu) rs104895501 0.00083
NM_001375808.2(LPIN2):c.1815G>A (p.Ser605=) rs143702044 0.00066
NM_001375808.2(LPIN2):c.2443-9C>T rs191749331 0.00047
NM_001375808.2(LPIN2):c.2568C>T (p.Leu856=) rs149862905 0.00045
NM_001375808.2(LPIN2):c.516C>T (p.Ala172=) rs150312425 0.00026
NM_001375808.2(LPIN2):c.2328-13A>T rs199830303 0.00017
NM_001375808.2(LPIN2):c.1793+17C>T rs188429587 0.00016
NM_001375808.2(LPIN2):c.2088-7T>G rs199713353 0.00011
NM_001375808.2(LPIN2):c.2371C>T (p.Leu791=) rs373520277 0.00011
NM_001375808.2(LPIN2):c.2327+14A>G rs370048111 0.00010
NM_001375808.2(LPIN2):c.289-16C>T rs759180126 0.00010
NM_001375808.2(LPIN2):c.2174+10C>T rs201227858 0.00007
NM_001375808.2(LPIN2):c.1011C>T (p.Ser337=) rs375422942 0.00006
NM_001375808.2(LPIN2):c.1339G>A (p.Val447Met) rs373758040 0.00006
NM_001375808.2(LPIN2):c.2650C>T (p.Arg884Ter) rs547662448 0.00005
NM_001375808.2(LPIN2):c.1281C>T (p.Pro427=) rs778559792 0.00004
NM_001375808.2(LPIN2):c.2316C>T (p.Ser772=) rs145270447 0.00003
NM_001375808.2(LPIN2):c.2547-11C>T rs776045621 0.00003
NM_001375808.2(LPIN2):c.540A>C (p.Thr180=) rs151135579 0.00003
NM_001375808.2(LPIN2):c.1347C>T (p.Ser449=) rs773074044 0.00002
NM_001375808.2(LPIN2):c.1814C>T (p.Ser605Leu) rs781778980 0.00002
NM_001375808.2(LPIN2):c.1299C>T (p.Pro433=) rs781673368 0.00001
NM_001375808.2(LPIN2):c.1720T>A (p.Ser574Thr) rs148779863 0.00001
NM_001375808.2(LPIN2):c.2443-14A>G rs749926941 0.00001
NM_001375808.2(LPIN2):c.2484A>G (p.Arg828=) rs761194035 0.00001
NM_001375808.2(LPIN2):c.-4A>G rs1555678614
NM_001375808.2(LPIN2):c.1621-18C>G rs375819924
NM_001375808.2(LPIN2):c.1794-9G>A rs587781026
NM_001375808.2(LPIN2):c.1812C>A (p.Ser604=) rs879254186
NM_001375808.2(LPIN2):c.193-9C>T rs1555677691
NM_001375808.2(LPIN2):c.1939-5A>G rs779830291
NM_001375808.2(LPIN2):c.2327+9C>A rs536913334
NM_001375808.2(LPIN2):c.2327+9C>T rs536913334
NM_001375808.2(LPIN2):c.2328-15_2328-10del rs770202563
NM_001375808.2(LPIN2):c.2400G>A (p.Pro800=) rs747097533
NM_001375808.2(LPIN2):c.2427T>C (p.Phe809=) rs1057520415
NM_001375808.2(LPIN2):c.2546+51T>A rs3737514
NM_001375808.2(LPIN2):c.288+63G>A
NM_001375808.2(LPIN2):c.289-95_289-94del rs10570659

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