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: 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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