List of variants in gene PIGN reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_176787.5(PIGN):c.685C>G (p.His229Asp)	rs9320001	0.79552
NM_176787.5(PIGN):c.1517G>A (p.Trp506Ter)	rs2146506059
NM_176787.5(PIGN):c.160C>T (p.Leu54Phe)	rs1599663316
NM_176787.5(PIGN):c.1694G>T (p.Arg565Leu)	rs201835155
NM_176787.5(PIGN):c.283C>T (p.Arg95Trp)	rs558341655
NM_176787.5(PIGN):c.491_492del (p.Glu164fs)	rs748817187

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