rs11545029
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs11545029(A;A) |
Make rs11545029(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 78386878 |
Gene | WWOX |
is a | snp |
is | mentioned by |
dbSNP | rs11545029 |
dbSNP (classic) | rs11545029 |
ClinGen | rs11545029 |
ebi | rs11545029 |
HLI | rs11545029 |
Exac | rs11545029 |
Gnomad | rs11545029 |
Varsome | rs11545029 |
LitVar | rs11545029 |
Map | rs11545029 |
PheGenI | rs11545029 |
Biobank | rs11545029 |
1000 genomes | rs11545029 |
hgdp | rs11545029 |
ensembl | rs11545029 |
geneview | rs11545029 |
scholar | rs11545029 |
rs11545029 | |
pharmgkb | rs11545029 |
gwascentral | rs11545029 |
openSNP | rs11545029 |
23andMe | rs11545029 |
SNPshot | rs11545029 |
SNPdbe | rs11545029 |
MSV3d | rs11545029 |
GWAS Ctlg | rs11545029 |
Merged from | Rs12918952 |
GMAF | 0.3269 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs11545029(A;A) rs11545029(T;T) |
Alt | rs11545029(A;A) rs11545029(T;T) |
Reference | Rs11545029(G;G) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | WWOX |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000016.9:g.78420775G>A |
CLNSRC | |
CLNACC | RCV000253370.2, |