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rs606231452

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231452(C;G)
Make rs606231452(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position1535392
GeneTMEM240
is asnp
is mentioned by
dbSNPrs606231452
ebirs606231452
HLIrs606231452
Exacrs606231452
Varsomers606231452
Maprs606231452
PheGenIrs606231452
hapmaprs606231452
1000 genomesrs606231452
hgdprs606231452
ensemblrs606231452
gopubmedrs606231452
geneviewrs606231452
scholarrs606231452
googlers606231452
pharmgkbrs606231452
gwascentralrs606231452
openSNPrs606231452
23andMers606231452
23andMe allrs606231452
SNP Nexus

SNPshotrs606231452
SNPdbers606231452
MSV3drs606231452
GWAS Ctlgrs606231452
Max Magnitude0
ClinVar
Risk rs606231452(G;G)
Alt rs606231452(G;G)
Reference rs606231452(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 21
Variation info
Gene TMEM240
CLNDBN Spinocerebellar ataxia 21
Reversed 1
HGVS NC_000001.10:g.1470772G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000148345.3,