List of variants in gene GNAS reported as likely benign by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_016592.5(GNAS):c.*42+26G>A	rs41305799	0.02679
NM_000516.7(GNAS):c.586-42G>A	rs1004902	0.01702
NM_000516.7(GNAS):c.213-268C>T	rs76801208	0.01562
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_000516.7(GNAS):c.531-295C>G	rs147630997	0.00742
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_080425.4(GNAS):c.1798C>G (p.Arg600Gly)	rs74897360	0.00538
NM_080425.4(GNAS):c.1395A>C (p.Pro465=)	rs56213454	0.00027
NM_080425.4(GNAS):c.1399G>T (p.Ala467Ser)	rs56371919	0.00018
NM_000516.7(GNAS):c.-18GCC[8] (p.Met1_Gly2insAlaAla)	rs745433225
NM_080425.4(GNAS):c.628G>C (p.Ala210Pro)	rs61749696

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