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rs606231451

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231451(C;T)
Make rs606231451(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position1535372
GeneTMEM240
is asnp
is mentioned by
dbSNPrs606231451
ebirs606231451
HLIrs606231451
Exacrs606231451
Varsomers606231451
Maprs606231451
PheGenIrs606231451
hapmaprs606231451
1000 genomesrs606231451
hgdprs606231451
ensemblrs606231451
gopubmedrs606231451
geneviewrs606231451
scholarrs606231451
googlers606231451
pharmgkbrs606231451
gwascentralrs606231451
openSNPrs606231451
23andMers606231451
23andMe allrs606231451
SNP Nexus

SNPshotrs606231451
SNPdbers606231451
MSV3drs606231451
GWAS Ctlgrs606231451
Max Magnitude0
ClinVar
Risk rs606231451(T;T)
Alt rs606231451(T;T)
Reference rs606231451(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene TMEM240
CLNDBN Spinocerebellar ataxia 21
Reversed 1
HGVS NC_000001.10:g.1470752G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000148344.3,