List of variants in gene C9 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001737.5(C9):c.355T>G (p.Cys119Gly)	rs121909593	0.00013
NM_001737.5(C9):c.460C>T (p.Arg154Ter)	rs144138616	0.00005
NM_001737.5(C9):c.871-2A>G	rs763129394	0.00001
NC_000005.9:g.(?_39306699)_(39331936_?)dup
NM_001737.5(C9):c.1209_1222del (p.Asp403fs)	rs767328870
NM_001737.5(C9):c.329-2A>G
NM_001737.5(C9):c.476+1G>C

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