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rs372245668

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372245668(C;T)
Make rs372245668(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position24658560
GeneTDP2
is asnp
is mentioned by
dbSNPrs372245668
ebirs372245668
HLIrs372245668
Exacrs372245668
Varsomers372245668
Maprs372245668
PheGenIrs372245668
hapmaprs372245668
1000 genomesrs372245668
hgdprs372245668
ensemblrs372245668
gopubmedrs372245668
geneviewrs372245668
scholarrs372245668
googlers372245668
pharmgkbrs372245668
gwascentralrs372245668
openSNPrs372245668
23andMers372245668
23andMe allrs372245668
SNP Nexus

SNPshotrs372245668
SNPdbers372245668
MSV3drs372245668
GWAS Ctlgrs372245668
Max Magnitude0
ClinVar
Risk rs372245668(T;T)
Alt rs372245668(T;T)
Reference rs372245668(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene TDP2
CLNDBN Spinocerebellar ataxia, autosomal recessive 23
Reversed 0
HGVS NC_000006.11:g.24658788C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000211705.1,