ClinVar Miner

List of variants in gene GNAS reported by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000516.7(GNAS):c.389A>G (p.Tyr130Cys)	rs2146184314
NM_000516.7(GNAS):c.658del (p.His220fs)	rs2517241190
NM_016592.5(GNAS):c.34C>T (p.Arg12Ter)	rs2085661524

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