rs16899066
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs16899066(C;C) |
Make rs16899066(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355803 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs16899066 |
dbSNP (classic) | rs16899066 |
ClinGen | rs16899066 |
ebi | rs16899066 |
HLI | rs16899066 |
Exac | rs16899066 |
Gnomad | rs16899066 |
Varsome | rs16899066 |
LitVar | rs16899066 |
Map | rs16899066 |
PheGenI | rs16899066 |
Biobank | rs16899066 |
1000 genomes | rs16899066 |
hgdp | rs16899066 |
ensembl | rs16899066 |
geneview | rs16899066 |
scholar | rs16899066 |
rs16899066 | |
pharmgkb | rs16899066 |
gwascentral | rs16899066 |
openSNP | rs16899066 |
23andMe | rs16899066 |
SNPshot | rs16899066 |
SNPdbe | rs16899066 |
MSV3d | rs16899066 |
GWAS Ctlg | rs16899066 |
GMAF | 0.01699 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs16899066(C;C) |
Alt | rs16899066(C;C) |
Reference | Rs16899066(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31323580T>C |
CLNSRC | |
CLNACC |