rs45504795
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs45504795(-;-) |
Make rs45504795(-;C) |
Reference | GRCh37.p5 37.3/137 |
Chromosome | 6 |
Position | 31324371 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs45504795 |
dbSNP (classic) | rs45504795 |
ClinGen | rs45504795 |
ebi | rs45504795 |
HLI | rs45504795 |
Exac | rs45504795 |
Gnomad | rs45504795 |
Varsome | rs45504795 |
LitVar | rs45504795 |
Map | rs45504795 |
PheGenI | rs45504795 |
Biobank | rs45504795 |
1000 genomes | rs45504795 |
hgdp | rs45504795 |
ensembl | rs45504795 |
geneview | rs45504795 |
scholar | rs45504795 |
rs45504795 | |
pharmgkb | rs45504795 |
gwascentral | rs45504795 |
openSNP | rs45504795 |
23andMe | rs45504795 |
SNPshot | rs45504795 |
SNPdbe | rs45504795 |
MSV3d | rs45504795 |
GWAS Ctlg | rs45504795 |
Status | Deleted |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs45504795(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324371delG |
CLNSRC | |
CLNACC |