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rs876657385

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657385(C;T)
Make rs876657385(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position85513857
GeneSNX14
is asnp
is mentioned by
dbSNPrs876657385
ebirs876657385
HLIrs876657385
Exacrs876657385
Varsomers876657385
Maprs876657385
PheGenIrs876657385
hapmaprs876657385
1000 genomesrs876657385
hgdprs876657385
ensemblrs876657385
gopubmedrs876657385
geneviewrs876657385
scholarrs876657385
googlers876657385
pharmgkbrs876657385
gwascentralrs876657385
openSNPrs876657385
23andMers876657385
23andMe allrs876657385
SNP Nexus

SNPshotrs876657385
SNPdbers876657385
MSV3drs876657385
GWAS Ctlgrs876657385
Max Magnitude0
ClinVar
Risk rs876657385(T;T)
Alt rs876657385(T;T)
Reference rs876657385(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SNX14
CLNDBN Spinocerebellar ataxia, autosomal recessive 20
Reversed 1
HGVS NC_000006.11:g.86223575G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170502.3,