ClinVar Miner

List of variants reported as likely benign for Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 16
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HGVS dbSNP
NM_015046.7(SETX):c.*168C>T
NM_015046.7(SETX):c.*2232T>C rs545456048
NM_015046.7(SETX):c.*2506T>C rs73545065
NM_015046.7(SETX):c.*319C>T rs1056912
NM_015046.7(SETX):c.*905A>G rs58327306
NM_015046.7(SETX):c.1693T>C (p.Phe565Leu) rs143982186
NM_015046.7(SETX):c.1880T>C (p.Met627Thr) rs199707503
NM_015046.7(SETX):c.2216G>A (p.Gly739Glu) rs36024203
NM_015046.7(SETX):c.2672T>C (p.Val891Ala) rs148181729
NM_015046.7(SETX):c.3103A>G (p.Lys1035Glu) rs117229601
NM_015046.7(SETX):c.3310C>G (p.Gln1104Glu) rs113831637
NM_015046.7(SETX):c.3992C>T (p.Pro1331Leu) rs11243731
NM_015046.7(SETX):c.4204A>T (p.Thr1402Ser) rs150421712
NM_015046.7(SETX):c.4660T>G (p.Cys1554Gly) rs112089123
NM_015046.7(SETX):c.7640T>C (p.Ile2547Thr) rs151117904
NM_015046.7(SETX):c.7724C>T (p.Pro2575Leu) rs34000644

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