ClinVar Miner

List of variants in gene GNAS reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_016592.5(GNAS):c.-52A>G rs1800900 0.57843
NM_016592.5(GNAS):c.*42+54A>G rs1800905 0.57266
NM_000516.7(GNAS):c.393C>T (p.Ile131=) rs7121 0.56988
NM_080425.4(GNAS):c.2068+89C>G rs73306256 0.43903
NM_000516.7(GNAS):c.432+93G>A rs3730168 0.35717
NM_000516.7(GNAS):c.258-138A>T rs2295583 0.30480
NM_000516.7(GNAS):c.531-132T>C rs919196 0.21645
NM_000516.7(GNAS):c.432+287A>G rs6026593 0.19311
NM_000516.7(GNAS):c.140-150G>A rs3730164 0.15261
NM_000516.7(GNAS):c.840-72C>T rs3730173 0.09640
NM_000516.7(GNAS):c.555C>T (p.Ile185=) rs8620 0.08427
NM_080425.4(GNAS):c.2068+180A>T rs75029190 0.08285
NM_080425.4(GNAS):c.1307C>A (p.Ala436Asp) rs61749698 0.07665
NM_000516.7(GNAS):c.433-18T>C rs3730170 0.07025
NM_016592.5(GNAS):c.-295C>G rs61558260 0.06254
NM_016592.5(GNAS):c.*42+21C>T rs1800904 0.06241
NM_000516.7(GNAS):c.1113C>T (p.Asn371=) rs8386 0.06127
NM_000516.7(GNAS):c.433-71G>T rs3730169 0.01978
NM_080425.4(GNAS):c.2068+169A>T rs115850041 0.01763
NM_000516.7(GNAS):c.257+159A>G rs80350825 0.01632
NM_000516.7(GNAS):c.*136G>A rs3730177 0.00553
NM_000516.7(GNAS):c.1039-127T>C rs234628
NM_000516.7(GNAS):c.140-247_140-243del rs148549965
NM_000516.7(GNAS):c.432C>T (p.Pro144=) rs11554266
NM_000516.7(GNAS):c.531-269G>A rs234629
NM_000516.7(GNAS):c.585+55C>G rs3730172
NM_080425.4(GNAS):c.-106T>G rs79335353
NM_080425.4(GNAS):c.1394_1395insCGACTCCGGGGCGGCCCGTGACGCCCCAGCCGATCC (p.Asp466_Ala467insSerGlyAlaAlaArgAspAlaProAlaAspProAsp) rs1196950915
NM_080425.4(GNAS):c.2068+160_2068+161insTT rs142555685

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