List of variants in gene GNAS reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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.238G>A (p.Ala80Thr)
NM_000516.7(GNAS):c.257+970_257+972del	rs1174800950
NM_000516.7(GNAS):c.565_568del (p.Asp189fs)	rs587776829

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