ClinVar Miner

List of variants in gene PLA2G6 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_003560.4(PLA2G6):c.-20C>A rs191263821 0.00121
NM_003560.4(PLA2G6):c.1615G>A (p.Gly539Ser) rs143826762 0.00092
NM_003560.4(PLA2G6):c.*541C>T rs45473603 0.00070
NM_003560.2(PLA2G6):c.*672G>A rs572000246 0.00066
NM_003560.4(PLA2G6):c.966C>T (p.His322=) rs144033740 0.00044
NM_003560.4(PLA2G6):c.2068G>A (p.Val690Ile) rs141777179 0.00041
NM_003560.4(PLA2G6):c.101C>T (p.Ser34Leu) rs147948449 0.00040
NM_003560.4(PLA2G6):c.416G>A (p.Arg139His) rs141825182 0.00038
NM_003560.4(PLA2G6):c.91G>A (p.Asp31Asn) rs150024227 0.00035
NM_003560.4(PLA2G6):c.956C>T (p.Thr319Met) rs149653983 0.00029
NM_003560.4(PLA2G6):c.325C>G (p.His109Asp) rs142530390 0.00028
NM_003560.4(PLA2G6):c.773C>T (p.Ser258Leu) rs147924368 0.00024
NM_003560.4(PLA2G6):c.439G>A (p.Ala147Thr) rs138672490 0.00020
NM_003560.4(PLA2G6):c.386T>C (p.Leu129Pro) rs374746113 0.00019
NM_003560.4(PLA2G6):c.441G>A (p.Ala147=) rs371920697 0.00019
NM_003560.4(PLA2G6):c.396C>T (p.Arg132=) rs146252218 0.00018
NM_003560.4(PLA2G6):c.1427C>T (p.Thr476Ile) rs146684391 0.00017
NM_003560.4(PLA2G6):c.2259C>T (p.Val753=) rs749966284 0.00014
NM_003560.4(PLA2G6):c.16C>T (p.Arg6Cys) rs143250889 0.00012
NM_003560.4(PLA2G6):c.*191C>T rs886057499 0.00011
NM_003560.4(PLA2G6):c.1725G>A (p.Thr575=) rs200599704 0.00010
NM_003560.4(PLA2G6):c.995G>C (p.Cys332Ser) rs780423461 0.00010
NM_003560.4(PLA2G6):c.895-11G>A rs371094406 0.00008
NM_003560.4(PLA2G6):c.1614C>T (p.Arg538=) rs373930150 0.00007
NM_003560.4(PLA2G6):c.-15C>T rs758224555 0.00006
NM_003560.4(PLA2G6):c.*160T>C rs886057500 0.00004
NM_003560.4(PLA2G6):c.*493C>G rs188998877 0.00004
NM_003560.4(PLA2G6):c.*515C>T rs1280474402 0.00004
NM_003560.4(PLA2G6):c.1267G>A (p.Ala423Thr) rs746217497 0.00004
NM_003560.4(PLA2G6):c.*473C>T rs886057498 0.00003
NM_003560.4(PLA2G6):c.*620G>A rs948625014 0.00003
NM_003560.4(PLA2G6):c.-31C>T rs376270953 0.00003
NM_003560.4(PLA2G6):c.1945C>T (p.Arg649Cys) rs746432450 0.00003
NM_003560.4(PLA2G6):c.1983G>A (p.Thr661=) rs150572286 0.00003
NM_003560.4(PLA2G6):c.448G>A (p.Glu150Lys) rs777548266 0.00003
NM_003560.4(PLA2G6):c.895-5C>T rs372128546 0.00003
NM_003560.4(PLA2G6):c.1205T>A (p.Ile402Asn) rs764199136 0.00002
NM_003560.4(PLA2G6):c.1348+10G>A rs761202760 0.00002
NM_003560.4(PLA2G6):c.155A>G (p.Asn52Ser) rs772131195 0.00002
NM_003560.4(PLA2G6):c.1648C>T (p.Arg550Trp) rs886057502 0.00002
NM_003560.4(PLA2G6):c.209G>A (p.Arg70Gln) rs11570607 0.00002
NM_003560.4(PLA2G6):c.2215G>C (p.Asp739His) rs587784349 0.00002
NM_003560.2(PLA2G6):c.*676T>C rs1175205623 0.00001
NM_003560.4(PLA2G6):c.*35C>T rs532364258 0.00001
NM_003560.4(PLA2G6):c.1414G>A (p.Asp472Asn) rs375874092 0.00001
NM_003560.4(PLA2G6):c.1531C>G (p.Leu511Val) rs886057503 0.00001
NM_003560.4(PLA2G6):c.1600A>G (p.Met534Val) rs748730147 0.00001
NM_003560.4(PLA2G6):c.2028C>T (p.Ile676=) rs561645994 0.00001
NM_003560.4(PLA2G6):c.67C>T (p.Arg23Trp) rs769876649 0.00001
NM_003560.4(PLA2G6):c.*548C>G rs866066890
NM_003560.4(PLA2G6):c.*565C>G rs886057497
NM_003560.4(PLA2G6):c.1904G>A (p.Arg635Gln) rs387906863
NM_003560.4(PLA2G6):c.1977C>T (p.Asn659=) rs201727354
NM_003560.4(PLA2G6):c.2030G>T (p.Arg677Leu) rs369038599
NM_003560.4(PLA2G6):c.2035-926G>A
NM_003560.4(PLA2G6):c.2035G>A (p.Gly679Ser) rs886057501
NM_003560.4(PLA2G6):c.2202+5G>A rs587784348
NM_003560.4(PLA2G6):c.2376C>A (p.His792Gln) rs751982449
NM_003560.4(PLA2G6):c.266C>A (p.Ser89Tyr) rs142715413
NM_003560.4(PLA2G6):c.776C>A (p.Ala259Asp) rs2088801961
NM_003560.4(PLA2G6):c.894+6T>G rs2088460355
NM_003560.4(PLA2G6):c.894+8G>A rs752942062
NM_003560.4(PLA2G6):c.991G>A (p.Asp331Asn) rs199935023

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