List of variants in gene GNAS reported as benign for not specified

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000516.7(GNAS):c.393C>T (p.Ile131=)	rs7121	0.56988
NM_000516.7(GNAS):c.555C>T (p.Ile185=)	rs8620	0.08427
NM_000516.7(GNAS):c.433-18T>C	rs3730170	0.07025
NM_000516.7(GNAS):c.1113C>T (p.Asn371=)	rs8386	0.06127
NM_016592.5(GNAS):c.294C>T (p.Pro98=)	rs1800902	0.04961
NM_080425.4(GNAS):c.627G>A (p.Lys209=)	rs74934823	0.03663
NM_080425.4(GNAS):c.1127C>T (p.Pro376Leu)	rs61749697	0.02257
NM_016592.5(GNAS):c.715C>A (p.Pro239Thr)	rs79527543	0.01288
NM_080425.4(GNAS):c.1376C>G (p.Pro459Arg)	rs148033592	0.01117
NM_080425.4(GNAS):c.525T>C (p.Ser175=)	rs114255910	0.00782
NM_080425.4(GNAS):c.500A>G (p.Asp167Gly)	rs61749695	0.00734
NM_000516.7(GNAS):c.951C>T (p.Arg317=)	rs75561530	0.00680
NM_000516.7(GNAS):c.384G>A (p.Val128=)	rs3730166	0.00609
NM_000516.7(GNAS):c.366C>T (p.Pro122=)	rs35287986	0.00583
NM_080425.4(GNAS):c.1798C>G (p.Arg600Gly)	rs74897360	0.00538
NM_080425.4(GNAS):c.1455C>A (p.Ala485=)	rs55890501	0.00388
NM_016592.5(GNAS):c.441G>A (p.Pro147=)	rs77400319	0.00146
NM_000516.7(GNAS):c.306G>A (p.Ala102=)	rs117849691	0.00131
NM_016592.5(GNAS):c.537G>A (p.Pro179=)	rs181594534	0.00072
NM_000516.7(GNAS):c.9C>T (p.Cys3=)	rs200810763	0.00061
NM_080425.4(GNAS):c.1524C>T (p.Ala508=)	rs111796234	0.00014
NM_000516.7(GNAS):c.90G>A (p.Leu30=)	rs144260225	0.00008
NM_000516.7(GNAS):c.576G>T (p.Pro192=)	rs558915293	0.00005
NM_000516.7(GNAS):c.432C>T (p.Pro144=)	rs11554266
NM_080425.4(GNAS):c.1188_1196dup (p.Ala400_Asp401insAlaProAla)	rs577386316
NM_080425.4(GNAS):c.1394_1395insCGACTCCGGGGCGGCCCGTGACGCCCCAGCCGATCC (p.Asp466_Ala467insSerGlyAlaAlaArgAspAlaProAlaAspProAsp)	rs1196950915

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