List of variants in gene PLA2G6 reported as pathogenic for not provided

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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_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln)	rs121908686	0.00009
NM_003560.4(PLA2G6):c.2370T>G (p.Tyr790Ter)	rs121908680	0.00006
NM_003560.4(PLA2G6):c.2221C>T (p.Arg741Trp)	rs530348521	0.00004
NM_003560.4(PLA2G6):c.2239C>T (p.Arg747Trp)	rs121908687	0.00003
NM_003560.4(PLA2G6):c.2370_2371del (p.Tyr790_Glu791delinsTer)	rs587784353	0.00003
NM_003560.4(PLA2G6):c.1894C>T (p.Arg632Trp)	rs121908683	0.00002
NM_003560.4(PLA2G6):c.2215G>C (p.Asp739His)	rs587784349	0.00002
NC_000022.10:g.38522454delG	rs587784329	0.00001
NM_003560.4(PLA2G6):c.1077G>A (p.Ser359=)	rs368497893	0.00001
NM_003560.4(PLA2G6):c.109C>T (p.Arg37Ter)	rs200075782	0.00001
NM_003560.4(PLA2G6):c.1427+1G>A	rs750939090	0.00001
NM_003560.4(PLA2G6):c.1627C>T (p.Arg543Cys)	rs753874848	0.00001
NM_003560.4(PLA2G6):c.1771C>T (p.Arg591Trp)	rs1043378899	0.00001
NM_003560.4(PLA2G6):c.1903C>T (p.Arg635Ter)	rs587784339	0.00001
NM_003560.4(PLA2G6):c.208C>T (p.Arg70Ter)	rs886039552	0.00001
NM_003560.4(PLA2G6):c.238G>A (p.Ala80Thr)	rs121908685	0.00001
NM_003560.4(PLA2G6):c.1019_1025del (p.Gly340fs)	rs797044903
NM_003560.4(PLA2G6):c.1186+1G>A	rs761815070
NM_003560.4(PLA2G6):c.1186+1G>T
NM_003560.4(PLA2G6):c.1501G>A (p.Glu501Lys)	rs587784332
NM_003560.4(PLA2G6):c.1648del (p.Arg550fs)
NM_003560.4(PLA2G6):c.1772G>A (p.Arg591Gln)	rs776713955
NM_003560.4(PLA2G6):c.1915del (p.Ala639fs)
NM_003560.4(PLA2G6):c.2070_2072del (p.Val691del)	rs587784343
NM_003560.4(PLA2G6):c.2098C>T (p.Gln700Ter)	rs587784346
NM_003560.4(PLA2G6):c.2251G>T (p.Glu751Ter)	rs1296348337
NM_003560.4(PLA2G6):c.2276+1G>A	rs1397030516
NM_003560.4(PLA2G6):c.2349G>A (p.Trp783Ter)	rs775386225
NM_003560.4(PLA2G6):c.319del (p.Leu107fs)	rs776376695
NM_003560.4(PLA2G6):c.643C>T (p.Gln215Ter)	rs2088813126
NM_003560.4(PLA2G6):c.671T>C (p.Leu224Pro)	rs2145803751
NM_003560.4(PLA2G6):c.673C>T (p.His225Tyr)	rs587784359
NM_003560.4(PLA2G6):c.729_740del (p.Ala244_Asn247del)	rs587784360
NM_003560.4(PLA2G6):c.755del (p.Asn252fs)	rs587784361
NM_003560.4(PLA2G6):c.857_858del (p.Tyr286fs)	rs2145780100
NM_003560.4(PLA2G6):c.991G>T (p.Asp331Tyr)	rs199935023

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