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rs869320748

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869320748(-;-)
Make rs869320748(-;A)
Make rs869320748(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position85549868
GeneSNX14
is asnp
is mentioned by
dbSNPrs869320748
ebirs869320748
HLIrs869320748
Exacrs869320748
Varsomers869320748
Maprs869320748
PheGenIrs869320748
hapmaprs869320748
1000 genomesrs869320748
hgdprs869320748
ensemblrs869320748
gopubmedrs869320748
geneviewrs869320748
scholarrs869320748
googlers869320748
pharmgkbrs869320748
gwascentralrs869320748
openSNPrs869320748
23andMers869320748
23andMe allrs869320748
SNP Nexus

SNPshotrs869320748
SNPdbers869320748
MSV3drs869320748
GWAS Ctlgrs869320748
Max Magnitude0
ClinVar
Risk rs869320748(A;A)
Alt rs869320748(A;A)
Reference rs869320748(;)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SNX14
CLNDBN Spinocerebellar ataxia, autosomal recessive 20
Reversed 1
HGVS NC_000006.11:g.86259587dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000170504.3,