rs794726680
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TT;TT) | 0 | common in clinvar |
Make rs794726680(-;-) |
Make rs794726680(-;TT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 43576703 |
Gene | ANO10 |
is a | snp |
is | mentioned by |
dbSNP | rs794726680 |
dbSNP (classic) | rs794726680 |
ClinGen | rs794726680 |
ebi | rs794726680 |
HLI | rs794726680 |
Exac | rs794726680 |
Gnomad | rs794726680 |
Varsome | rs794726680 |
LitVar | rs794726680 |
Map | rs794726680 |
PheGenI | rs794726680 |
Biobank | rs794726680 |
1000 genomes | rs794726680 |
hgdp | rs794726680 |
ensembl | rs794726680 |
geneview | rs794726680 |
scholar | rs794726680 |
rs794726680 | |
pharmgkb | rs794726680 |
gwascentral | rs794726680 |
openSNP | rs794726680 |
23andMe | rs794726680 |
SNPshot | rs794726680 |
SNPdbe | rs794726680 |
MSV3d | rs794726680 |
GWAS Ctlg | rs794726680 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794726680(-;-) |
Alt | rs794726680(-;-) |
Reference | Rs794726680(TT;TT) |
Significance | Pathogenic |
Disease | Spinocerebellar ataxia |
Variation | info |
Gene | ANO10 |
CLNDBN | Spinocerebellar ataxia, autosomal recessive 10 |
Reversed | 1 |
HGVS | NC_000003.11:g.43618195_43618196delAA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000024052.5, |