ClinVar Miner

List of variants in gene LPIN2 reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_001375808.2(LPIN2):c.822+304A>G rs115314461 0.01770
NM_001375808.2(LPIN2):c.1793+268C>T rs142329002 0.01449
NM_001375808.2(LPIN2):c.1793+270A>T rs145211520 0.01448
NM_001375808.2(LPIN2):c.1456+170A>G rs79206481 0.01120
NM_001375808.2(LPIN2):c.-9-94A>T rs78634942 0.00940
NM_001375808.2(LPIN2):c.1268+154C>T rs116250233 0.00864
NM_001375808.2(LPIN2):c.2175-299T>C rs148084447 0.00837
NM_001375808.2(LPIN2):c.1801G>A (p.Glu601Lys) rs61735393 0.00824
NM_001375808.2(LPIN2):c.822+171A>T rs77797831 0.00807
NM_001375808.2(LPIN2):c.1711-97A>C rs143574323 0.00757
NM_001375808.2(LPIN2):c.1793+98G>A rs112137712 0.00698
NM_001375808.2(LPIN2):c.2175-163G>T rs112147026 0.00606
NM_001375808.2(LPIN2):c.2546+145T>C rs182217640 0.00576
NM_001375808.2(LPIN2):c.1939-159T>C rs149482453 0.00544
NM_001375808.2(LPIN2):c.1621-203_1621-193dup rs111745076 0.00542
NM_001375808.2(LPIN2):c.1793+23G>A rs111549482 0.00542
NM_001375808.2(LPIN2):c.1710+218G>A rs112797038 0.00541
NM_001375808.2(LPIN2):c.1168+120_1168+121del rs1303968835 0.00461
NM_001375808.2(LPIN2):c.193-93G>C rs559520487 0.00296
NM_001375808.2(LPIN2):c.699-24C>T rs148154982 0.00272
NM_001375808.2(LPIN2):c.193-228G>A rs767274148 0.00262
NM_001375808.2(LPIN2):c.1510C>T (p.Leu504Phe) rs104895500 0.00253
NM_001375808.2(LPIN2):c.1735T>C (p.Ser579Pro) rs150022314 0.00221
NM_001375808.2(LPIN2):c.-10+1381T>C rs566304730 0.00176
NM_001375808.2(LPIN2):c.2443-22C>T rs117806728 0.00142
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser) rs80338805 0.00142
NM_001375808.2(LPIN2):c.1268+224G>A rs186067725 0.00108
NM_001375808.2(LPIN2):c.1876C>T (p.Pro626Ser) rs150806357 0.00083
NM_001375808.2(LPIN2):c.1043C>T (p.Pro348Leu) rs34676691 0.00051
NM_001375808.2(LPIN2):c.446C>T (p.Pro149Leu) rs147615538 0.00038
NM_001375808.2(LPIN2):c.2610C>T (p.Ser870=) rs145412418 0.00025
NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=) rs187572602 0.00025
NM_001375808.2(LPIN2):c.1168+6C>T rs200130790 0.00024
NM_001375808.2(LPIN2):c.1132C>T (p.Pro378Ser) rs201678207 0.00018
NM_001375808.2(LPIN2):c.2535A>C (p.Gly845=) rs186864136 0.00012
NM_001375808.2(LPIN2):c.1169-3C>T rs200259086 0.00011
NM_001375808.2(LPIN2):c.588A>G (p.Ala196=) rs1020661683 0.00007
NM_001375808.2(LPIN2):c.1281C>T (p.Pro427=) rs778559792 0.00004
NM_001375808.2(LPIN2):c.1456+4C>G rs373685201 0.00004
NM_001375808.2(LPIN2):c.2088-10G>A rs374043211 0.00004
NM_001375808.2(LPIN2):c.2316C>T (p.Ser772=) rs145270447 0.00003
NM_001375808.2(LPIN2):c.*12_*15del rs752690266 0.00002
NM_001375808.2(LPIN2):c.1362C>T (p.Ser454=) rs371484024 0.00002
NM_001375808.2(LPIN2):c.1332A>G (p.Pro444=) rs1297660489 0.00001
NM_001375808.2(LPIN2):c.2493C>T (p.Thr831=) rs1167923626 0.00001
NM_001375808.2(LPIN2):c.*90C>T rs547359065
NM_001375808.2(LPIN2):c.1026G>A (p.Val342=) rs1232642116
NM_001375808.2(LPIN2):c.1168+120C>T rs868816773
NM_001375808.2(LPIN2):c.1169-7del rs746626720
NM_001375808.2(LPIN2):c.1457-267dup rs201649931
NM_001375808.2(LPIN2):c.1812C>A (p.Ser604=) rs879254186
NM_001375808.2(LPIN2):c.1830A>C (p.Ser610=)
NM_001375808.2(LPIN2):c.2087+9A>C rs1598522453
NM_001375808.2(LPIN2):c.2088-229G>A rs116088791
NM_001375808.2(LPIN2):c.2088-66C>G rs116485090
NM_001375808.2(LPIN2):c.2174+218_2174+219del rs533090312
NM_001375808.2(LPIN2):c.2442+129C>T rs116178219
NM_001375808.2(LPIN2):c.2621G>T (p.Cys874Phe) rs201160155
NM_001375808.2(LPIN2):c.273G>A (p.Glu91=)
NM_001375808.2(LPIN2):c.288+54C>T rs116804085
NM_001375808.2(LPIN2):c.289-96_289-94del rs10570659
NM_001375808.2(LPIN2):c.699-13_699-12dup rs775605400
NM_001375808.2(LPIN2):c.948C>T (p.Ser316=)

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