rs9260155
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs9260155(C;C) |
Make rs9260155(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943462 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs9260155 |
dbSNP (classic) | rs9260155 |
ClinGen | rs9260155 |
ebi | rs9260155 |
HLI | rs9260155 |
Exac | rs9260155 |
Gnomad | rs9260155 |
Varsome | rs9260155 |
LitVar | rs9260155 |
Map | rs9260155 |
PheGenI | rs9260155 |
Biobank | rs9260155 |
1000 genomes | rs9260155 |
hgdp | rs9260155 |
ensembl | rs9260155 |
geneview | rs9260155 |
scholar | rs9260155 |
rs9260155 | |
pharmgkb | rs9260155 |
gwascentral | rs9260155 |
openSNP | rs9260155 |
23andMe | rs9260155 |
SNPshot | rs9260155 |
SNPdbe | rs9260155 |
MSV3d | rs9260155 |
GWAS Ctlg | rs9260155 |
GMAF | 0.2888 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs9260155(A;A) rs9260155(C;C) rs9260155(G;G) |
Alt | rs9260155(A;A) rs9260155(C;C) rs9260155(G;G) |
Reference | Rs9260155(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911239T; NC_000006.11:g.29911239T>A; NC_000006.11:g.29911239T>C; NC_000006.11:g.29911239T>G |
CLNSRC | |
CLNACC |