rs45452896
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs45452896(A;A) |
Make rs45452896(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31357081 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs45452896 |
dbSNP (classic) | rs45452896 |
ClinGen | rs45452896 |
ebi | rs45452896 |
HLI | rs45452896 |
Exac | rs45452896 |
Gnomad | rs45452896 |
Varsome | rs45452896 |
LitVar | rs45452896 |
Map | rs45452896 |
PheGenI | rs45452896 |
Biobank | rs45452896 |
1000 genomes | rs45452896 |
hgdp | rs45452896 |
ensembl | rs45452896 |
geneview | rs45452896 |
scholar | rs45452896 |
rs45452896 | |
pharmgkb | rs45452896 |
gwascentral | rs45452896 |
openSNP | rs45452896 |
23andMe | rs45452896 |
SNPshot | rs45452896 |
SNPdbe | rs45452896 |
MSV3d | rs45452896 |
GWAS Ctlg | rs45452896 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs45452896(A;A) |
Alt | rs45452896(A;A) |
Reference | Rs45452896(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324858C>T |
CLNSRC | |
CLNACC |