ClinVar Miner

List of variants in gene LPIN1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_145693.2(LPIN1):c.-69445T>G rs4374337 0.94841
NM_001349206.2(LPIN1):c.1806+203T>C rs7607755 0.66949
NM_001349206.2(LPIN1):c.1806+41G>T rs7561070 0.66842
NM_001261428.3(LPIN1):c.39G>C (p.Glu13Asp) rs4669769 0.55034
NM_001261428.3(LPIN1):c.138+161T>C rs4668739 0.38670
NM_001261428.3(LPIN1):c.82-108T>C rs12465629 0.38623
NM_001261428.3(LPIN1):c.138+50A>T rs12465630 0.38617
NM_001349206.2(LPIN1):c.958-273A>G rs11695702 0.33159
NM_001349206.2(LPIN1):c.1549+133A>G rs13392363 0.32245
NM_001261427.3(LPIN1):c.9+255T>G rs72773975 0.29965
NM_001261427.3(LPIN1):c.-71-277A>C rs56788115 0.29920
NM_001349206.2(LPIN1):c.2517+181T>C rs2716609 0.27739
NM_001349206.2(LPIN1):c.192+17C>T rs10209969 0.26135
NM_001349206.2(LPIN1):c.597-308C>T rs2358042 0.26068
NM_001349206.2(LPIN1):c.1643+231del rs60603136 0.23383
NM_145693.2(LPIN1):c.-69443G>A rs12477584 0.20254
NM_001349206.2(LPIN1):c.1264+273C>T rs56124251 0.19262
NM_001349206.2(LPIN1):c.2249+251C>A rs62114965 0.18851
NM_001261428.3(LPIN1):c.113G>A (p.Arg38Gln) rs4614906 0.17664
NM_001261428.3(LPIN1):c.138+26G>A rs4640359 0.17649
NM_001261428.3(LPIN1):c.138+74G>A rs10182021 0.15581
NM_001261428.3(LPIN1):c.82-299G>T rs13398067 0.15539
NM_001349206.2(LPIN1):c.1264+222A>G rs7587836 0.15514
NM_001349206.2(LPIN1):c.193-47C>T rs45509591 0.14634
NM_001349206.2(LPIN1):c.596+152G>T rs72773999 0.14566
NM_001261428.3(LPIN1):c.82-127G>A rs10179409 0.14119
NM_001349206.2(LPIN1):c.596+176C>G rs72774000 0.13950
NM_001349206.2(LPIN1):c.1358+245G>A rs3762583 0.10904
NM_001261428.3(LPIN1):c.81+275G>A rs11695025 0.10317
NM_001349206.2(LPIN1):c.552C>T (p.Ile184=) rs11538448 0.09460
NM_001261428.3(LPIN1):c.81+165G>A rs11694975 0.09406
NM_001349206.2(LPIN1):c.2250-272T>C rs79161028 0.08703
NM_001349206.2(LPIN1):c.2403-346A>G rs57450916 0.08251
NM_001261428.3(LPIN1):c.138+25C>T rs62113260 0.07534
NM_001349206.2(LPIN1):c.-9-21T>G rs7599595 0.06747
NM_001349206.2(LPIN1):c.657G>A (p.Leu219=) rs59909741 0.06723
NM_001261428.3(LPIN1):c.82-160T>C rs73181378 0.06136
NM_001349206.2(LPIN1):c.1265-280A>G rs4129755 0.05675
NM_001349206.2(LPIN1):c.2517+259A>G rs10495584 0.05545
NM_001349206.2(LPIN1):c.596+141G>A rs111726318 0.04415
NM_001349206.2(LPIN1):c.2402+237C>T rs75560733 0.04359
NM_001349206.2(LPIN1):c.-9-161C>T rs73917123 0.04334
NM_001349206.2(LPIN1):c.2358G>C (p.Gly786=) rs61732581 0.04121
NM_001349206.2(LPIN1):c.2517+226A>G rs2577258 0.03917
NM_001349206.2(LPIN1):c.1936C>T (p.Pro646Ser) rs4669781 0.03693
NM_001349206.2(LPIN1):c.1807-212G>C rs78580932 0.03204
NM_001349206.2(LPIN1):c.192+171C>T rs56187608 0.03021
NM_001349206.2(LPIN1):c.192+190G>A rs75403163 0.02840
NM_001349206.2(LPIN1):c.2622-171A>G rs7340376 0.02788
NM_001261428.3(LPIN1):c.82-297C>G rs56122279 0.02473
NM_001349206.2(LPIN1):c.192+197A>C rs78800346 0.02415
NM_001349206.2(LPIN1):c.1359-194T>G rs114514177 0.02225
NM_001349206.2(LPIN1):c.723-171T>C rs145221282 0.02174
NM_001349206.2(LPIN1):c.830+36A>G rs75785575 0.02131
NM_001349206.2(LPIN1):c.2622-172C>T rs76364927 0.01842
NM_001349206.2(LPIN1):c.1588G>A (p.Val530Met) rs33997857 0.01739
NM_001349206.2(LPIN1):c.420C>T (p.Ile140=) rs75945731 0.01127
NM_001349206.2(LPIN1):c.696G>C (p.Ser232=) rs145180224 0.00818
NM_001349206.2(LPIN1):c.1225C>G (p.Gln409Glu) rs146529487 0.00097
NM_001261428.3(LPIN1):c.-69G>A rs74422146
NM_001349206.2(LPIN1):c.-9-14del rs3214670
NM_001349206.2(LPIN1):c.1643+231_1643+232del rs1553435317
NM_001349206.2(LPIN1):c.1714-100dup rs78343196
NM_001349206.2(LPIN1):c.2162+54del rs111652164
NM_001349206.2(LPIN1):c.2403-228C>T rs2716610
NM_001349206.2(LPIN1):c.723-156TA[2] rs200414823
NM_001349206.2(LPIN1):c.958TCT[2] (p.Ser322del) rs149564563

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