ClinVar Miner

List of variants in gene GABRG2 reported as likely benign by GeneDx

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Total variants: 29
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HGVS dbSNP
NM_198903.2(GABRG2):c.*20A>C rs796052501
NM_198903.2(GABRG2):c.1035A>G (p.Thr345=) rs1398214382
NM_198903.2(GABRG2):c.1042+6A>G rs375294947
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.107+6A>G rs868452487
NM_198903.2(GABRG2):c.1074C>T (p.Leu358=) rs749531013
NM_198903.2(GABRG2):c.108-182G>A rs146492172
NM_198903.2(GABRG2):c.1122G>A (p.Ala374=) rs371601817
NM_198903.2(GABRG2):c.1134T>C (p.Phe378=) rs1057521488
NM_198903.2(GABRG2):c.11C>T (p.Pro4Leu) rs375295110
NM_198903.2(GABRG2):c.1248+14T>C rs779125212
NM_198903.2(GABRG2):c.1404T>C (p.Cys468=) rs141138508
NM_198903.2(GABRG2):c.1440G>A (p.Gly480=) rs150727562
NM_198903.2(GABRG2):c.1509G>A (p.Leu503=) rs765904792
NM_198903.2(GABRG2):c.15T>C (p.Asn5=) rs1057522820
NM_198903.2(GABRG2):c.162A>G (p.Thr54=) rs748255945
NM_198903.2(GABRG2):c.259+19C>T rs758196181
NM_198903.2(GABRG2):c.259+60A>T rs78369083
NM_198903.2(GABRG2):c.260-16_260-15del rs747283752
NM_198903.2(GABRG2):c.333C>T (p.Tyr111=) rs777192588
NM_198903.2(GABRG2):c.37G>A (p.Val13Ile) rs796052502
NM_198903.2(GABRG2):c.420C>T (p.Asn140=) rs1581350860
NM_198903.2(GABRG2):c.525T>C (p.Asp175=) rs770485021
NM_198903.2(GABRG2):c.548+14A>G rs1057521821
NM_198903.2(GABRG2):c.574T>C (p.Leu192=) rs1554098050
NM_198903.2(GABRG2):c.752-8C>T rs779617978
NM_198903.2(GABRG2):c.99C>T (p.Leu33=) rs368162707

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