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rs606231455

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231455(C;T)
Make rs606231455(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position1535370
GeneTMEM240
is asnp
is mentioned by
dbSNPrs606231455
ebirs606231455
HLIrs606231455
Exacrs606231455
Varsomers606231455
Maprs606231455
PheGenIrs606231455
hapmaprs606231455
1000 genomesrs606231455
hgdprs606231455
ensemblrs606231455
gopubmedrs606231455
geneviewrs606231455
scholarrs606231455
googlers606231455
pharmgkbrs606231455
gwascentralrs606231455
openSNPrs606231455
23andMers606231455
23andMe allrs606231455
SNP Nexus

SNPshotrs606231455
SNPdbers606231455
MSV3drs606231455
GWAS Ctlgrs606231455
Max Magnitude0
ClinVar
Risk rs606231455(T;T)
Alt rs606231455(T;T)
Reference rs606231455(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene TMEM240
CLNDBN Spinocerebellar ataxia 21
Reversed 1
HGVS NC_000001.10:g.1470750G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000148348.3,