ClinVar Miner

List of variants in gene LPIN2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001375808.2(LPIN2):c.-9-186A>T rs652587 0.57561
NM_001375808.2(LPIN2):c.1711-220C>A rs602233 0.52957
NM_001375808.2(LPIN2):c.1793+260A>G rs8096970 0.40168
NM_001375808.2(LPIN2):c.1793+259C>T rs8091774 0.38611
NM_001375808.2(LPIN2):c.2175-253A>G rs12458532 0.37314
NM_001375808.2(LPIN2):c.823-112C>T rs9961969 0.36632
NM_001375808.2(LPIN2):c.1268+152C>T rs9635812 0.34097
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.2328-132A>G rs2282636 0.30195
NM_001375808.2(LPIN2):c.1620+208A>G rs3745011 0.15428
NM_001375808.2(LPIN2):c.-10+1498C>T rs78132553 0.08877
NM_001375808.2(LPIN2):c.-10+1522A>G rs79931488 0.08873
NM_001375808.2(LPIN2):c.1793+242G>A rs73936863 0.07521
NM_001375808.2(LPIN2):c.1269-249C>T rs3786401 0.06935
NM_001375808.2(LPIN2):c.1168+290C>T rs7229067 0.05540
NM_001375808.2(LPIN2):c.2547-47C>T rs16944043 0.05084
NM_001375808.2(LPIN2):c.590+127T>C rs75643393 0.04498
NM_001375808.2(LPIN2):c.823-203G>A rs9962809 0.03760
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.1456+29A>G rs16944068 0.03261
NM_001375808.2(LPIN2):c.192+209A>G rs73936876 0.03186
NM_001375808.2(LPIN2):c.591-79G>C rs73375270 0.02952
NM_001375808.2(LPIN2):c.1168+11G>C rs79439091 0.02576
NM_001375808.2(LPIN2):c.1168+331A>G rs149731727 0.02379
NM_001375808.2(LPIN2):c.2443-276G>A rs77444753 0.02330
NM_001375808.2(LPIN2):c.1168+40T>C rs73936870 0.02313
NM_001375808.2(LPIN2):c.1794-140A>G rs58792754 0.02303
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.590+6A>G rs73375280 0.00505
NM_001375808.2(LPIN2):c.2174+17_2174+18insAT rs368009098 0.00452
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.2443-9C>T rs191749331 0.00047
NM_001375808.2(LPIN2):c.2568C>T (p.Leu856=) rs149862905 0.00045
NM_001375808.2(LPIN2):c.2445T>C (p.Asp815=) rs140249737 0.00021
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.1011C>T (p.Ser337=) rs375422942 0.00006
NM_001375808.2(LPIN2):c.608C>T (p.Ser203Phe) rs144555528 0.00006
NM_001375808.2(LPIN2):c.1456+4C>G rs373685201 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.795G>A (p.Thr265=) rs373300544 0.00001
NM_001375808.2(LPIN2):c.-9-128_-9-123del rs17881253
NM_001375808.2(LPIN2):c.1168+146_1168+147del rs71366618
NM_001375808.2(LPIN2):c.1168+147del rs71366618
NM_001375808.2(LPIN2):c.1457-98_1457-96del rs143599992
NM_001375808.2(LPIN2):c.1793+170del rs3841746
NM_001375808.2(LPIN2):c.1794-9G>A rs587781026
NM_001375808.2(LPIN2):c.192+122dup rs376940122
NM_001375808.2(LPIN2):c.193-288_193-286del rs3837908
NM_001375808.2(LPIN2):c.2327+66G>A rs76543111
NM_001375808.2(LPIN2):c.2443-38C>A rs377133832
NM_001375808.2(LPIN2):c.2546+51T>A rs3737514
NM_001375808.2(LPIN2):c.289-94del rs10570659
NM_001375808.2(LPIN2):c.289-95_289-94del rs10570659
NM_001375808.2(LPIN2):c.698+20_698+22del rs778249776
NM_014646.2:c.+3C>T

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