ClinVar Miner

List of variants in gene GABRG2 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_198904.4(GABRG2):c.631+1248A>G rs211035 0.82291
NM_198904.4(GABRG2):c.632-1175A>G rs211034 0.69820
NM_198904.4(GABRG2):c.588C>T (p.Asn196=) rs211037 0.31557
NM_198904.4(GABRG2):c.315C>T (p.Asn105=) rs11135176 0.07676
NM_198904.4(GABRG2):c.354G>A (p.Ala118=) rs61735412 0.01575
NM_198904.4(GABRG2):c.328-20T>G rs74810777 0.01496
NM_198904.4(GABRG2):c.631+1284G>T rs148215078 0.00925
NM_198904.4(GABRG2):c.360G>A (p.Thr120=) rs77298346 0.00541
NM_198904.4(GABRG2):c.632-1262C>A rs114972096 0.00517
NM_198904.4(GABRG2):c.717A>G (p.Gln239=) rs78261481 0.00489
NM_198904.4(GABRG2):c.259+20G>A rs200011382 0.00063
NM_198904.4(GABRG2):c.798T>C (p.Phe266=) rs115126975 0.00063
NM_198904.4(GABRG2):c.631+18T>A rs145582456 0.00050
NM_198904.4(GABRG2):c.922+20G>A rs11575991 0.00029
NM_198904.4(GABRG2):c.768C>T (p.Ser256=) rs201672465 0.00027
NM_198904.4(GABRG2):c.107+12C>T rs369466385 0.00024
NM_198904.4(GABRG2):c.769+20A>C rs182866753 0.00024
NM_198904.4(GABRG2):c.1236C>T (p.Tyr412=) rs749951528 0.00018
NM_198904.4(GABRG2):c.243T>A (p.Leu81=) rs143295869 0.00014
NM_198904.4(GABRG2):c.1254C>T (p.Asp418=) rs113085352 0.00009
NM_198904.4(GABRG2):c.769+18A>G rs2422105 0.00007
NM_198904.4(GABRG2):c.632-1212C>T rs587780948 0.00004
NM_198904.4(GABRG2):c.327+12A>C rs188717038
NM_198904.4(GABRG2):c.631+1209TTGTT[5] rs1247520830
NM_198904.4(GABRG2):c.631+1283G>A rs143065876
NM_198904.4(GABRG2):c.840T>C (p.Tyr280=) rs558779533

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