List of variants reported as likely benign for Amyotrophic neuralgia

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001113491.2(SEPTIN9):c.*479C>A	rs28364841	0.00664
NM_001113491.2(SEPTIN9):c.722-6424G>C	rs200871334	0.00025
NM_001113491.2(SEPTIN9):c.146C>A (p.Thr49Asn)	rs549141429	0.00004
NM_001113491.2(SEPTIN9):c.819G>A (p.Pro273=)	rs751622773	0.00001

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