List of variants in gene PIGL reported as uncertain significance for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_004278.4(PIGL):c.424C>A (p.Leu142Met)	rs115958467	0.00486
NM_004278.4(PIGL):c.526+10G>A	rs138410893	0.00121
NM_004278.4(PIGL):c.337G>T (p.Asp113Tyr)	rs114670807	0.00083
NM_004278.4(PIGL):c.500T>C (p.Leu167Pro)	rs145303331	0.00062
NM_004278.4(PIGL):c.446G>C (p.Gly149Ala)	rs140211194	0.00017
NM_004278.4(PIGL):c.439G>A (p.Asp147Asn)	rs148238492	0.00016
NM_004278.4(PIGL):c.493A>C (p.Arg165=)	rs184077858	0.00014
NM_004278.4(PIGL):c.595T>C (p.Leu199=)	rs114176862	0.00014
NM_004278.4(PIGL):c.354A>G (p.Pro118=)	rs149094276	0.00010
NM_004278.4(PIGL):c.542C>T (p.Thr181Met)	rs748231024	0.00010
NM_004278.4(PIGL):c.627C>T (p.Phe209=)	rs146164310	0.00008
NM_004278.4(PIGL):c.336-2A>G	rs369230457	0.00007
NM_004278.4(PIGL):c.*184A>C	rs886052643	0.00006
NM_004278.4(PIGL):c.*324A>G	rs886052645	0.00004
NM_004278.4(PIGL):c.263G>A (p.Arg88His)	rs755380500	0.00004
NM_004278.4(PIGL):c.426+14T>C	rs138467285	0.00003
NM_004278.4(PIGL):c.420C>T (p.Ile140=)	rs374713933	0.00002
NM_004278.4(PIGL):c.724C>T (p.Arg242Trp)	rs377632512	0.00002
NM_004278.4(PIGL):c.*318C>A	rs146448001	0.00001
NM_004278.4(PIGL):c.130C>T (p.Leu44=)	rs776742163	0.00001
NM_004278.4(PIGL):c.296T>G (p.Leu99Trp)	rs1179113684	0.00001
NM_004278.4(PIGL):c.30G>T (p.Ala10=)	rs147669920	0.00001
NM_004278.4(PIGL):c.480G>A (p.Leu160=)	rs114697377	0.00001
NM_004278.4(PIGL):c.534T>C (p.Ser178=)	rs114145762	0.00001
NM_004278.4(PIGL):c.535G>A (p.Val179Met)	rs116591352	0.00001
NM_004278.4(PIGL):c.540C>T (p.Leu180=)	rs115695383	0.00001
NM_004278.4(PIGL):c.*185A>C	rs886052644
NM_004278.4(PIGL):c.169T>C (p.Phe57Leu)	rs587784324
NM_004278.4(PIGL):c.176C>A (p.Pro59His)	rs1057518948
NM_004278.4(PIGL):c.258_259del (p.Glu86fs)	rs763616470
NM_004278.4(PIGL):c.262C>G (p.Arg88Gly)	rs1064795400
NM_004278.4(PIGL):c.398A>G (p.Gln133Arg)	rs749202572
NM_004278.4(PIGL):c.426+8G>A	rs145914582
NM_004278.4(PIGL):c.535G>T (p.Val179Leu)	rs116591352
NM_004278.4(PIGL):c.652C>G (p.Gln218Glu)	rs139004722
NM_004278.4(PIGL):c.725G>C (p.Arg242Pro)	rs750654333

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