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rs876657387

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657387(A;A)
Make rs876657387(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position85567567
GeneSNX14
is asnp
is mentioned by
dbSNPrs876657387
ebirs876657387
HLIrs876657387
Exacrs876657387
Varsomers876657387
Maprs876657387
PheGenIrs876657387
hapmaprs876657387
1000 genomesrs876657387
hgdprs876657387
ensemblrs876657387
gopubmedrs876657387
geneviewrs876657387
scholarrs876657387
googlers876657387
pharmgkbrs876657387
gwascentralrs876657387
openSNPrs876657387
23andMers876657387
23andMe allrs876657387
SNP Nexus

SNPshotrs876657387
SNPdbers876657387
MSV3drs876657387
GWAS Ctlgrs876657387
Max Magnitude0
ClinVar
Risk rs876657387(A;A)
Alt rs876657387(A;A)
Reference rs876657387(T;T)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SNX14
CLNDBN Spinocerebellar ataxia, autosomal recessive 20
Reversed 1
HGVS NC_000006.11:g.86277285A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170507.3,