rs17880291
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs17880291(G;G) |
Make rs17880291(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29944785 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs17880291 |
dbSNP (classic) | rs17880291 |
ClinGen | rs17880291 |
ebi | rs17880291 |
HLI | rs17880291 |
Exac | rs17880291 |
Gnomad | rs17880291 |
Varsome | rs17880291 |
LitVar | rs17880291 |
Map | rs17880291 |
PheGenI | rs17880291 |
Biobank | rs17880291 |
1000 genomes | rs17880291 |
hgdp | rs17880291 |
ensembl | rs17880291 |
geneview | rs17880291 |
scholar | rs17880291 |
rs17880291 | |
pharmgkb | rs17880291 |
gwascentral | rs17880291 |
openSNP | rs17880291 |
23andMe | rs17880291 |
SNPshot | rs17880291 |
SNPdbe | rs17880291 |
MSV3d | rs17880291 |
GWAS Ctlg | rs17880291 |
GMAF | 0.1465 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs17880291(G;G) |
Alt | rs17880291(G;G) |
Reference | Rs17880291(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29912562T>G |
CLNSRC | |
CLNACC |