List of variants in gene PIGV reported as benign for not provided

Minimum submission review status:		Collection method:
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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_017837.4(PIGV):c.-338A>C	rs113400508	0.05897
NM_017837.4(PIGV):c.1201-190G>A	rs74827250	0.05818
NM_017837.4(PIGV):c.*210A>G	rs57189461	0.05712
NM_017837.4(PIGV):c.615C>T (p.Asn205=)	rs34512715	0.00995
NM_017837.4(PIGV):c.101C>T (p.Pro34Leu)	rs139246652	0.00505
NM_017837.4(PIGV):c.348G>A (p.Leu116=)	rs148662665	0.00096
NM_017837.4(PIGV):c.*149G>A	rs3754360	0.00091
NM_017837.4(PIGV):c.1369C>T (p.Leu457Phe)	rs143676075	0.00068
NM_017837.4(PIGV):c.809G>A (p.Arg270His)	rs149379900	0.00005
NM_017837.4(PIGV):c.-333C>T	rs118069986
NM_017837.4(PIGV):c.1200+196C>A	rs115960004

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