Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231134

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231134(A;G)
Make rs606231134(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position152321898
GeneSYNE1
is asnp
is mentioned by
dbSNPrs606231134
ebirs606231134
HLIrs606231134
Exacrs606231134
Varsomers606231134
Maprs606231134
PheGenIrs606231134
hapmaprs606231134
1000 genomesrs606231134
hgdprs606231134
ensemblrs606231134
gopubmedrs606231134
geneviewrs606231134
scholarrs606231134
googlers606231134
pharmgkbrs606231134
gwascentralrs606231134
openSNPrs606231134
23andMers606231134
23andMe allrs606231134
SNP Nexus

SNPshotrs606231134
SNPdbers606231134
MSV3drs606231134
GWAS Ctlgrs606231134
Max Magnitude0
ClinVar
Risk rs606231134(G;G)
Alt rs606231134(G;G)
Reference rs606231134(A;A)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SYNE1
CLNDBN Spinocerebellar ataxia, autosomal recessive 8
Reversed 1
HGVS NC_000006.11:g.152643033T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002416.3,