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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP
NM_198903.2(GABRG2):c.1042+20G>A	rs11575991
NM_198903.2(GABRG2):c.107+12C>T	rs369466385
NM_198903.2(GABRG2):c.1356C>T (p.Tyr452=)	rs749951528
NM_198903.2(GABRG2):c.1374C>T (p.Asp458=)	rs113085352
NM_198903.2(GABRG2):c.243T>A (p.Leu81=)	rs143295869
NM_198903.2(GABRG2):c.259+20G>A	rs200011382
NM_198903.2(GABRG2):c.315C>T (p.Asn105=)	rs11135176
NM_198903.2(GABRG2):c.327+12A>C	rs188717038
NM_198903.2(GABRG2):c.328-20T>G	rs74810777
NM_198903.2(GABRG2):c.360G>A (p.Thr120=)	rs77298346
NM_198903.2(GABRG2):c.588C>T (p.Asn196=)	rs211037
NM_198903.2(GABRG2):c.631+18T>A	rs145582456
NM_198903.2(GABRG2):c.632-28TTGTT[5]	rs1247520830
NM_198903.2(GABRG2):c.678G>A (p.Ser226=)	rs143065876
NM_198903.2(GABRG2):c.679G>T (p.Ala227Ser)	rs148215078
NM_198903.2(GABRG2):c.705C>A (p.Gly235=)	rs114972096
NM_198903.2(GABRG2):c.751+4C>T	rs587780948
NM_198903.2(GABRG2):c.837A>G (p.Gln279=)	rs78261481
NM_198903.2(GABRG2):c.888C>T (p.Ser296=)	rs201672465
NM_198903.2(GABRG2):c.889+18A>G	rs2422105
NM_198903.2(GABRG2):c.889+20A>C	rs182866753
NM_198903.2(GABRG2):c.918T>C (p.Phe306=)	rs115126975
NM_198903.2(GABRG2):c.960T>C (p.Tyr320=)	rs558779533

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