ClinVar Miner

List of variants in gene GABRG2 reported as likely benign for not provided

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Total variants: 17
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HGVS dbSNP
NM_198903.2(GABRG2):c.1062A>G (p.Thr354=) rs377502016
NM_198903.2(GABRG2):c.107+11C>A rs376576632
NM_198903.2(GABRG2):c.107+223T>G rs149245576
NM_198903.2(GABRG2):c.108-182G>A rs146492172
NM_198903.2(GABRG2):c.1273-8C>G rs771660227
NM_198903.2(GABRG2):c.1290C>A (p.Ile430=) rs1312081444
NM_198903.2(GABRG2):c.1302A>G (p.Ser434=) rs1458041410
NM_198903.2(GABRG2):c.1374C>T (p.Asp458=) rs113085352
NM_198903.2(GABRG2):c.1470C>T (p.Asp490=) rs202246006
NM_198903.2(GABRG2):c.1518G>T (p.Leu506=) rs1581463326
NM_198903.2(GABRG2):c.243T>A (p.Leu81=) rs143295869
NM_198903.2(GABRG2):c.259+60A>T rs78369083
NM_198903.2(GABRG2):c.420C>T (p.Asn140=) rs1581350860
NM_198903.2(GABRG2):c.752-8C>T rs779617978
NM_198903.2(GABRG2):c.928A>C (p.Arg310=) rs796052520
NM_198903.2(GABRG2):c.99C>T (p.Leu33=) rs368162707
NM_198904.4(GABRG2):c.972A>G (p.Lys324=)

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