rs763903197
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs763903197(A;A) |
Make rs763903197(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 219421343 |
Gene | DES |
is a | snp |
is | mentioned by |
dbSNP | rs763903197 |
dbSNP (classic) | rs763903197 |
ClinGen | rs763903197 |
ebi | rs763903197 |
HLI | rs763903197 |
Exac | rs763903197 |
Gnomad | rs763903197 |
Varsome | rs763903197 |
LitVar | rs763903197 |
Map | rs763903197 |
PheGenI | rs763903197 |
Biobank | rs763903197 |
1000 genomes | rs763903197 |
hgdp | rs763903197 |
ensembl | rs763903197 |
geneview | rs763903197 |
scholar | rs763903197 |
rs763903197 | |
pharmgkb | rs763903197 |
gwascentral | rs763903197 |
openSNP | rs763903197 |
23andMe | rs763903197 |
SNPshot | rs763903197 |
SNPdbe | rs763903197 |
MSV3d | rs763903197 |
GWAS Ctlg | rs763903197 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763903197(A;A) |
Alt | rs763903197(A;A) |
Reference | Rs763903197(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | DES |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.220286065G>A |
CLNSRC | |
CLNACC | RCV000183353.2, RCV000278818.1, |