rs41545616
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs41545616(C;C) |
Make rs41545616(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355154 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs41545616 |
dbSNP (classic) | rs41545616 |
ClinGen | rs41545616 |
ebi | rs41545616 |
HLI | rs41545616 |
Exac | rs41545616 |
Gnomad | rs41545616 |
Varsome | rs41545616 |
LitVar | rs41545616 |
Map | rs41545616 |
PheGenI | rs41545616 |
Biobank | rs41545616 |
1000 genomes | rs41545616 |
hgdp | rs41545616 |
ensembl | rs41545616 |
geneview | rs41545616 |
scholar | rs41545616 |
rs41545616 | |
pharmgkb | rs41545616 |
gwascentral | rs41545616 |
openSNP | rs41545616 |
23andMe | rs41545616 |
SNPshot | rs41545616 |
SNPdbe | rs41545616 |
MSV3d | rs41545616 |
GWAS Ctlg | rs41545616 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41545616(C;C) |
Alt | rs41545616(C;C) |
Reference | Rs41545616(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31322931A>G |
CLNSRC | |
CLNACC |