List of variants in gene GNAS reported as uncertain significance by Revvity Omics, Revvity

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000516.7(GNAS):c.437T>C (p.Phe146Ser)
NM_000516.7(GNAS):c.702G>C (p.Trp234Cys)	rs2091303526
NM_080425.4(GNAS):c.416T>C (p.Met139Thr)

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