rs41556912
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41556912(-;-) |
Make rs41556912(-;C) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 6 |
Position | 29911059 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41556912 |
dbSNP (classic) | rs41556912 |
ClinGen | rs41556912 |
ebi | rs41556912 |
HLI | rs41556912 |
Exac | rs41556912 |
Gnomad | rs41556912 |
Varsome | rs41556912 |
LitVar | rs41556912 |
Map | rs41556912 |
PheGenI | rs41556912 |
Biobank | rs41556912 |
1000 genomes | rs41556912 |
hgdp | rs41556912 |
ensembl | rs41556912 |
geneview | rs41556912 |
scholar | rs41556912 |
rs41556912 | |
pharmgkb | rs41556912 |
gwascentral | rs41556912 |
openSNP | rs41556912 |
23andMe | rs41556912 |
SNPshot | rs41556912 |
SNPdbe | rs41556912 |
MSV3d | rs41556912 |
GWAS Ctlg | rs41556912 |
Status | Deleted |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs41556912(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911059delC |
CLNSRC | |
CLNACC |