List of variants in gene GNAS reported as uncertain significance by Mendelics

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_080425.4(GNAS):c.505C>T (p.Pro169Ser)	rs746247739	0.00007
NM_080425.4(GNAS):c.1397_1398insC (p.Ala467fs)	rs1178804802	0.00001
NM_080425.4(GNAS):c.803C>G (p.Pro268Arg)	rs2145566990

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