rs372245668
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs372245668(C;T) |
Make rs372245668(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 24658560 |
Gene | TDP2 |
is a | snp |
is | mentioned by |
dbSNP | rs372245668 |
dbSNP (classic) | rs372245668 |
ClinGen | rs372245668 |
ebi | rs372245668 |
HLI | rs372245668 |
Exac | rs372245668 |
Gnomad | rs372245668 |
Varsome | rs372245668 |
LitVar | rs372245668 |
Map | rs372245668 |
PheGenI | rs372245668 |
Biobank | rs372245668 |
1000 genomes | rs372245668 |
hgdp | rs372245668 |
ensembl | rs372245668 |
geneview | rs372245668 |
scholar | rs372245668 |
rs372245668 | |
pharmgkb | rs372245668 |
gwascentral | rs372245668 |
openSNP | rs372245668 |
23andMe | rs372245668 |
SNPshot | rs372245668 |
SNPdbe | rs372245668 |
MSV3d | rs372245668 |
GWAS Ctlg | rs372245668 |
Max Magnitude | 0 |
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, |