rs17882753
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs17882753(C;T) |
Make rs17882753(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29944817 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs17882753 |
dbSNP (classic) | rs17882753 |
ClinGen | rs17882753 |
ebi | rs17882753 |
HLI | rs17882753 |
Exac | rs17882753 |
Gnomad | rs17882753 |
Varsome | rs17882753 |
LitVar | rs17882753 |
Map | rs17882753 |
PheGenI | rs17882753 |
Biobank | rs17882753 |
1000 genomes | rs17882753 |
hgdp | rs17882753 |
ensembl | rs17882753 |
geneview | rs17882753 |
scholar | rs17882753 |
rs17882753 | |
pharmgkb | rs17882753 |
gwascentral | rs17882753 |
openSNP | rs17882753 |
23andMe | rs17882753 |
SNPshot | rs17882753 |
SNPdbe | rs17882753 |
MSV3d | rs17882753 |
GWAS Ctlg | rs17882753 |
GMAF | 0.2107 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs17882753(T;T) |
Alt | rs17882753(T;T) |
Reference | Rs17882753(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29912594C>T |
CLNSRC | |
CLNACC |