List of variants reported as likely benign for Epilepsy, childhood absence 2

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.354G>A (p.Ala118=)	rs61735412	0.01699
NM_198904.4(GABRG2):c.*794A>G	rs73316347	0.00873
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.*343A>G	rs41275341	0.00432
NM_198904.4(GABRG2):c.*385G>A	rs185169107	0.00360
NM_198904.4(GABRG2):c.*261G>A	rs148001179	0.00153
NM_198904.4(GABRG2):c.*1636T>C	rs551794496	0.00113
NM_198904.4(GABRG2):c.*2095C>G	rs138297122	0.00105
NM_198904.4(GABRG2):c.*1518A>G	rs567153845	0.00035
NM_198904.4(GABRG2):c.768C>T (p.Ser256=)	rs201672465	0.00015
NM_198904.4(GABRG2):c.*797G>T	rs118064447	0.00001
NM_198904.4(GABRG2):c.*441T>C	rs188825588

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