rs41557912
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs41557912(G;G) |
Make rs41557912(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29945424 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41557912 |
dbSNP (classic) | rs41557912 |
ClinGen | rs41557912 |
ebi | rs41557912 |
HLI | rs41557912 |
Exac | rs41557912 |
Gnomad | rs41557912 |
Varsome | rs41557912 |
LitVar | rs41557912 |
Map | rs41557912 |
PheGenI | rs41557912 |
Biobank | rs41557912 |
1000 genomes | rs41557912 |
hgdp | rs41557912 |
ensembl | rs41557912 |
geneview | rs41557912 |
scholar | rs41557912 |
rs41557912 | |
pharmgkb | rs41557912 |
gwascentral | rs41557912 |
openSNP | rs41557912 |
23andMe | rs41557912 |
SNPshot | rs41557912 |
SNPdbe | rs41557912 |
MSV3d | rs41557912 |
GWAS Ctlg | rs41557912 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41557912(G;G) |
Alt | rs41557912(G;G) |
Reference | Rs41557912(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29913201T>G |
CLNSRC | |
CLNACC |