List of variants in gene GNAS reported as likely benign by Ambry Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_080425.4(GNAS):c.154G>A (p.Glu52Lys)	rs527488103	0.00022
NM_080425.4(GNAS):c.1343A>C (p.Asp448Ala)	rs776846313	0.00018
NM_000516.7(GNAS):c.530+11G>A	rs74474807	0.00017
NM_080425.4(GNAS):c.1700A>G (p.Glu567Gly)	rs200585625	0.00005
NM_080425.4(GNAS):c.969C>T (p.Val323=)	rs189777461	0.00004
NM_080425.4(GNAS):c.757A>G (p.Ser253Gly)	rs2145566367
NM_080425.4(GNAS):c.957C>T (p.Asp319=)

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