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rs786205229

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205229(C;T)
Make rs786205229(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position85543737
GeneSNX14
is asnp
is mentioned by
dbSNPrs786205229
ebirs786205229
HLIrs786205229
Exacrs786205229
Varsomers786205229
Maprs786205229
PheGenIrs786205229
hapmaprs786205229
1000 genomesrs786205229
hgdprs786205229
ensemblrs786205229
gopubmedrs786205229
geneviewrs786205229
scholarrs786205229
googlers786205229
pharmgkbrs786205229
gwascentralrs786205229
openSNPrs786205229
23andMers786205229
23andMe allrs786205229
SNP Nexus

SNPshotrs786205229
SNPdbers786205229
MSV3drs786205229
GWAS Ctlgrs786205229
Max Magnitude0
ClinVar
Risk rs786205229(T;T)
Alt rs786205229(T;T)
Reference rs786205229(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SNX14
CLNDBN Spinocerebellar ataxia, autosomal recessive 20
Reversed 1
HGVS NC_000006.11:g.86253455G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170506.3,