rs41549012
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs41549012(A;G) |
Make rs41549012(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943131 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41549012 |
dbSNP (classic) | rs41549012 |
ClinGen | rs41549012 |
ebi | rs41549012 |
HLI | rs41549012 |
Exac | rs41549012 |
Gnomad | rs41549012 |
Varsome | rs41549012 |
LitVar | rs41549012 |
Map | rs41549012 |
PheGenI | rs41549012 |
Biobank | rs41549012 |
1000 genomes | rs41549012 |
hgdp | rs41549012 |
ensembl | rs41549012 |
geneview | rs41549012 |
scholar | rs41549012 |
rs41549012 | |
pharmgkb | rs41549012 |
gwascentral | rs41549012 |
openSNP | rs41549012 |
23andMe | rs41549012 |
SNPshot | rs41549012 |
SNPdbe | rs41549012 |
MSV3d | rs41549012 |
GWAS Ctlg | rs41549012 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41549012(G;G) |
Alt | rs41549012(G;G) |
Reference | Rs41549012(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910908A>G |
CLNSRC | |
CLNACC |