ClinVar Miner

List of variants in gene GP9 reported as pathogenic by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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)
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Total variants: 2

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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.337del (p.Cys113fs)	rs1297298519	0.00001

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