rs10412199
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs10412199(A;A) |
Make rs10412199(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 3927773 |
Gene | ATCAY |
is a | snp |
is | mentioned by |
dbSNP | rs10412199 |
dbSNP (classic) | rs10412199 |
ClinGen | rs10412199 |
ebi | rs10412199 |
HLI | rs10412199 |
Exac | rs10412199 |
Gnomad | rs10412199 |
Varsome | rs10412199 |
LitVar | rs10412199 |
Map | rs10412199 |
PheGenI | rs10412199 |
Biobank | rs10412199 |
1000 genomes | rs10412199 |
hgdp | rs10412199 |
ensembl | rs10412199 |
geneview | rs10412199 |
scholar | rs10412199 |
rs10412199 | |
pharmgkb | rs10412199 |
gwascentral | rs10412199 |
openSNP | rs10412199 |
23andMe | rs10412199 |
SNPshot | rs10412199 |
SNPdbe | rs10412199 |
MSV3d | rs10412199 |
GWAS Ctlg | rs10412199 |
GMAF | 0.4288 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21782286] |
Trait | |
Title | A genome-wide association study of aging. |
Risk Allele | G |
P-val | 0.000003 |
Odds Ratio | 1.1000 [NR] |
ClinVar | |
---|---|
Risk | rs10412199(A;A) |
Alt | rs10412199(A;A) |
Reference | Rs10412199(G;G) |
Significance | Non-pathogenic |
Disease | Cerebellar ataxia |
Variation | info |
Gene | ATCAY |
CLNDBN | Cerebellar ataxia, cayman type |
Reversed | 0 |
HGVS | NC_000019.9:g.3927771G>A |
CLNSRC | |
CLNACC | RCV000263045.1, |