List of variants reported as likely benign for hereditary hyperekplexia by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004211.5(SLC6A5):c.342C>G (p.Pro114=)	rs61736605	0.00773
NM_020806.5(GPHN):c.800A>G (p.Asn267Ser)	rs41285470	0.00586
NM_001321967.2(ATAD1):c.657C>G (p.Leu219=)	rs116195084	0.00347
NM_001353921.2(ARHGEF9):c.1225A>G (p.Ile409Val)	rs56110425	0.00016
NM_000824.5(GLRB):c.298-19G>T	rs371067472
NM_000824.5(GLRB):c.904+4A>T	rs76714257
NM_020806.5(GPHN):c.1797T>C (p.Asp599=)	rs41285476

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