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rs876657386

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657386(G;T)
Make rs876657386(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position85530191
GeneSNX14
is asnp
is mentioned by
dbSNPrs876657386
ebirs876657386
HLIrs876657386
Exacrs876657386
Varsomers876657386
Maprs876657386
PheGenIrs876657386
hapmaprs876657386
1000 genomesrs876657386
hgdprs876657386
ensemblrs876657386
gopubmedrs876657386
geneviewrs876657386
scholarrs876657386
googlers876657386
pharmgkbrs876657386
gwascentralrs876657386
openSNPrs876657386
23andMers876657386
23andMe allrs876657386
SNP Nexus

SNPshotrs876657386
SNPdbers876657386
MSV3drs876657386
GWAS Ctlgrs876657386
Max Magnitude0
ClinVar
Risk rs876657386(T;T)
Alt rs876657386(T;T)
Reference rs876657386(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SNX14
CLNDBN Spinocerebellar ataxia, autosomal recessive 20
Reversed 1
HGVS NC_000006.11:g.86239909C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170505.4,