ClinVar Miner

List of variants in gene GNAS reported as uncertain significance by Division of Human Genetics, Children's Hospital of Philadelphia

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_080425.4(GNAS):c.1455C>A (p.Ala485=)	rs55890501	0.00388
NM_080425.4(GNAS):c.1200C>A (p.Ala400=)	rs908810796	0.00001

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