ClinVar Miner

List of variants in gene GABRB3 reported as likely benign for not specified

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_021912.5(GABRB3):c.31C>T (p.Pro11Ser) rs25409 0.00354
NM_000814.6(GABRB3):c.835+8C>T rs75812437 0.00031
NM_021912.5(GABRB3):c.80+19G>A rs536031008 0.00029
NM_021912.5(GABRB3):c.80+18C>T rs376837906 0.00024
NM_000814.6(GABRB3):c.585C>T (p.Gly195=) rs781294125 0.00015
NM_000814.6(GABRB3):c.1113G>A (p.Ser371=) rs139370891 0.00010
NM_000814.6(GABRB3):c.-23C>G rs889516195 0.00007
NM_000814.6(GABRB3):c.357C>T (p.Pro119=) rs370237352 0.00006
NM_000814.6(GABRB3):c.321G>T (p.Thr107=) rs367761610 0.00003
NM_000814.6(GABRB3):c.836-20C>T rs369364757 0.00003
NM_000814.6(GABRB3):c.753T>C (p.Tyr251=) rs150534186 0.00002
NM_021912.5(GABRB3):c.80+10G>A rs763316211 0.00002
NM_000814.6(GABRB3):c.1104G>C (p.Leu368=) rs777145235 0.00001
NM_000814.6(GABRB3):c.183C>G (p.Val61=) rs778097525 0.00001
NM_000814.6(GABRB3):c.81-11C>T rs759375301 0.00001
NM_000814.6(GABRB3):c.1005C>G (p.Gly335=) rs74907974
NM_000814.6(GABRB3):c.154C>T (p.Leu52=) rs1057524415
NM_000814.6(GABRB3):c.300T>C (p.Ser100=) rs975508044
NM_021912.4(GABRB3):c.-42G>C rs1057522017
NM_021912.4(GABRB3):c.-44G>C rs372201190
NM_021912.4(GABRB3):c.-44G>T rs372201190

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