Variants in gene PLA2G6 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003560.4(PLA2G6):c.209+16C>T	rs2267368	0.07814
NM_003560.4(PLA2G6):c.172G>A (p.Val58Ile)	rs11570605	0.01488
NM_003560.4(PLA2G6):c.1743-137G>A	rs55679135	0.00993
NM_003560.4(PLA2G6):c.1027G>A (p.Ala343Thr)	rs11570680	0.00890
NM_003560.4(PLA2G6):c.2340C>T (p.Asn780=)	rs138683183	0.00691
NM_003560.4(PLA2G6):c.495G>C (p.Gly165=)	rs150190277	0.00372
NM_003560.4(PLA2G6):c.972G>A (p.Ala324=)	rs147755372	0.00249
NM_003560.4(PLA2G6):c.990C>T (p.Phe330=)	rs146241431	0.00167
NM_003560.4(PLA2G6):c.2417C>G (p.Pro806Arg)	rs140758033	0.00021
NM_003560.4(PLA2G6):c.1742+12C>T	rs11570739	0.00009
NM_003560.4(PLA2G6):c.898G>A (p.Ala300Thr)	rs528966598	0.00004

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