List of variants in gene GABRG2 reported as benign for childhood absence epilepsy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.631+1248A>G	rs211035	0.82291
NM_198904.4(GABRG2):c.*661T>A	rs424740	0.44730
NM_198904.4(GABRG2):c.*609C>T	rs418210	0.32390
NM_198904.4(GABRG2):c.588C>T (p.Asn196=)	rs211037	0.31659
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.*1497C>T	rs11956247	0.01779
NM_198904.4(GABRG2):c.354G>A (p.Ala118=)	rs61735412	0.01699
NM_198904.4(GABRG2):c.328-20T>G	rs74810777	0.01604
NM_198904.4(GABRG2):c.*1974G>A	rs150875037	0.00909
NM_198904.4(GABRG2):c.360G>A (p.Thr120=)	rs77298346	0.00541
NM_198904.4(GABRG2):c.717A>G (p.Gln239=)	rs78261481	0.00489
NM_198904.4(GABRG2):c.798T>C (p.Phe266=)	rs115126975	0.00067
NM_198904.4(GABRG2):c.259+20G>A	rs200011382	0.00063
NM_198904.4(GABRG2):c.631+18T>A	rs145582456	0.00054
NM_198904.4(GABRG2):c.922+20G>A	rs11575991	0.00029
NM_198904.4(GABRG2):c.769+20A>C	rs182866753	0.00024
NM_198904.4(GABRG2):c.107+12C>T	rs369466385	0.00018
NM_198904.4(GABRG2):c.768C>T (p.Ser256=)	rs201672465	0.00015
NM_198904.4(GABRG2):c.769+18A>G	rs2422105	0.00007
NM_198904.4(GABRG2):c.409T>C (p.Leu137=)	rs200828542	0.00006
NM_198904.4(GABRG2):c.582G>A (p.Leu194=)	rs781498456	0.00002
NM_198904.4(GABRG2):c.1002G>A (p.Ala334=)	rs371601817	0.00001
NM_198904.4(GABRG2):c.17T>C (p.Ile6Thr)	rs759392289	0.00001
NM_198904.4(GABRG2):c.840T>C (p.Tyr280=)	rs558779533

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