rs57694264
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs57694264(A;A) |
Make rs57694264(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 219421517 |
Gene | DES |
is a | snp |
is | mentioned by |
dbSNP | rs57694264 |
dbSNP (classic) | rs57694264 |
ClinGen | rs57694264 |
ebi | rs57694264 |
HLI | rs57694264 |
Exac | rs57694264 |
Gnomad | rs57694264 |
Varsome | rs57694264 |
LitVar | rs57694264 |
Map | rs57694264 |
PheGenI | rs57694264 |
Biobank | rs57694264 |
1000 genomes | rs57694264 |
hgdp | rs57694264 |
ensembl | rs57694264 |
geneview | rs57694264 |
scholar | rs57694264 |
rs57694264 | |
pharmgkb | rs57694264 |
gwascentral | rs57694264 |
openSNP | rs57694264 |
23andMe | rs57694264 |
SNPshot | rs57694264 |
SNPdbe | rs57694264 |
MSV3d | rs57694264 |
GWAS Ctlg | rs57694264 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs57694264(A;A) |
Alt | rs57694264(A;A) |
Reference | Rs57694264(G;G) |
Significance | Untested |
Disease | not provided |
Variation | info |
Gene | DES |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.220286239G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000056780.3, |