rs9260191
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs9260191(A;G) |
Make rs9260191(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29944621 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs9260191 |
dbSNP (classic) | rs9260191 |
ClinGen | rs9260191 |
ebi | rs9260191 |
HLI | rs9260191 |
Exac | rs9260191 |
Gnomad | rs9260191 |
Varsome | rs9260191 |
LitVar | rs9260191 |
Map | rs9260191 |
PheGenI | rs9260191 |
Biobank | rs9260191 |
1000 genomes | rs9260191 |
hgdp | rs9260191 |
ensembl | rs9260191 |
geneview | rs9260191 |
scholar | rs9260191 |
rs9260191 | |
pharmgkb | rs9260191 |
gwascentral | rs9260191 |
openSNP | rs9260191 |
23andMe | rs9260191 |
SNPshot | rs9260191 |
SNPdbe | rs9260191 |
MSV3d | rs9260191 |
GWAS Ctlg | rs9260191 |
Merged from | Rs113824204 |
GMAF | 0.4867 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs9260191(G;G) rs9260191(T;T) |
Alt | rs9260191(G;G) rs9260191(T;T) |
Reference | Rs9260191(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29912398A>G |
CLNSRC | |
CLNACC |