List of variants reported as likely benign for hereditary hyperekplexia by Illumina Laboratory Services, Illumina

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000171.4(GLRA1):c.1108G>A (p.Gly370Ser)	rs116474260	0.00939
NM_000171.4(GLRA1):c.-164C>T	rs529450119	0.00169
NM_000171.4(GLRA1):c.50T>C (p.Phe17Ser)	rs376426309	0.00009
NM_000824.5(GLRB):c.423T>C (p.Pro141=)	rs145564477	0.00004
NM_000171.4(GLRA1):c.198C>T (p.Asn66=)	rs200606738	0.00003
NM_000171.4(GLRA1):c.185-9G>A	rs371382193	0.00001
NM_000171.4(GLRA1):c.585C>T (p.Ile195=)	rs370809444

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