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

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.260-183G>A	rs2963170	0.99807
NM_198904.4(GABRG2):c.631+1248A>G	rs211035	0.82291
NM_198904.4(GABRG2):c.632-1175A>G	rs211034	0.69579
NM_198904.4(GABRG2):c.632-160C>T	rs211030	0.69577
NM_198904.4(GABRG2):c.632-1087C>T	rs211033	0.69533
NM_198904.4(GABRG2):c.631+1046C>T	rs211036	0.44553
NM_198904.4(GABRG2):c.588C>T (p.Asn196=)	rs211037	0.31659
NM_198904.4(GABRG2):c.1128+99C>A	rs211014	0.29903
NM_198904.4(GABRG2):c.770-81A>G	rs17060112	0.14022
NM_198904.4(GABRG2):c.770-230A>T	rs2272600	0.13225
NM_198904.4(GABRG2):c.632-1164G>A	rs34281163	0.12783
NM_198904.4(GABRG2):c.632-1264G>T	rs41311629	0.10834
NM_198904.4(GABRG2):c.315C>T (p.Asn105=)	rs11135176	0.07676
NM_198904.4(GABRG2):c.-154C>T	rs3219203	0.05943
NM_198904.4(GABRG2):c.548+189T>G	rs76029468	0.04369
NM_198904.4(GABRG2):c.548+306C>T	rs76872907	0.03075
NM_198904.4(GABRG2):c.354G>A (p.Ala118=)	rs61735412	0.01699
NM_198904.4(GABRG2):c.631+1284G>T	rs148215078	0.00925
NM_198904.4(GABRG2):c.*1427C>T	rs375013278	0.00037
NM_198904.4(GABRG2):c.*296G>T	rs1025917717	0.00035
NM_198904.4(GABRG2):c.922+6A>G	rs375294947	0.00023
NM_198904.4(GABRG2):c.768C>T (p.Ser256=)	rs201672465	0.00015
NM_198904.4(GABRG2):c.1122A>G (p.Lys374=)	rs776166431	0.00011
NM_198904.4(GABRG2):c.1153-7G>A	rs372884176	0.00007
NM_198904.4(GABRG2):c.135C>T (p.Asp45=)	rs375308385	0.00007
NM_198904.4(GABRG2):c.632-6C>T	rs199883385	0.00006
NM_198904.4(GABRG2):c.219G>A (p.Leu73=)	rs753076158	0.00004
NM_198904.4(GABRG2):c.631+1283G>A	rs143065876
NM_198904.4(GABRG2):c.631+275del	rs34875047
NM_198904.4(GABRG2):c.922+108A>C	rs12520992

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