List of variants in gene GP9 reported as likely pathogenic for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000174.5(GP9):c.182A>G (p.Asn61Ser)	rs5030764	0.00076
NM_000174.5(GP9):c.259T>C (p.Trp87Arg)	rs766253334
NM_000174.5(GP9):c.404G>T (p.Cys135Phe)	rs769561588
NM_000174.5(GP9):c.429G>A (p.Trp143Ter)
NM_000174.5(GP9):c.70T>C (p.Cys24Arg)	rs28933378

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