Variants in gene PLA2G6 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_003560.4(PLA2G6):c.956C>T (p.Thr319Met)	rs149653983	0.00029
NM_003560.4(PLA2G6):c.386T>C (p.Leu129Pro)	rs374746113	0.00019
NM_003560.4(PLA2G6):c.2129G>A (p.Arg710His)	rs147455037	0.00010
NM_003560.4(PLA2G6):c.1495G>A (p.Ala499Thr)	rs141045127	0.00006
NM_003560.4(PLA2G6):c.1898C>T (p.Ala633Val)	rs201657455	0.00001
NM_003560.4(PLA2G6):c.2128C>T (p.Arg710Cys)	rs587784347	0.00001
NM_003560.4(PLA2G6):c.2249G>A (p.Cys750Tyr)	rs751225193	0.00001
NM_003560.4(PLA2G6):c.1506G>C (p.Lys502Asn)	rs1555988382
NM_003560.4(PLA2G6):c.1547C>T (p.Ala516Val)
NM_003560.4(PLA2G6):c.1778C>T (p.Pro593Leu)	rs1451486649
NM_003560.4(PLA2G6):c.1904G>A (p.Arg635Gln)	rs387906863
NM_003560.4(PLA2G6):c.668C>T (p.Pro223Leu)	rs776753796
NM_003560.4(PLA2G6):c.757G>A (p.Gly253Ser)	rs745643715

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