List of variants reported as benign for Epilepsy, idiopathic generalized, susceptibility to, 13

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001127644.2(GABRA1):c.1059+15G>A	rs2279020	0.62825
NM_001127644.2(GABRA1):c.*1506A>C	rs998754	0.60031
NM_001127644.2(GABRA1):c.*470A>G	rs2290732	0.59993
NM_000806.5(GABRA1):c.-441A>G	rs11576001	0.29650
NM_001127644.2(GABRA1):c.156T>C (p.Gly52=)	rs1129647	0.23538
NM_001127644.2(GABRA1):c.-142A>G	rs12658835	0.18269
NM_001127644.2(GABRA1):c.-31C>T	rs4608967	0.13210
NM_001127644.2(GABRA1):c.*1929T>C	rs2290733	0.01265

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