List of variants reported as pathogenic for Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_023077.3(COA7):c.17A>G (p.Asp6Gly)	rs780572767	0.00001
NM_023077.3(COA7):c.410A>G (p.Tyr137Cys)	rs961876891	0.00001
NM_023077.3(COA7):c.247+1G>T	rs1197945739
NM_023077.3(COA7):c.431del (p.Gly144fs)	rs1558102464
NM_023077.3(COA7):c.446G>T (p.Ser149Ile)	rs1558102448

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