rs41564218
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41564218(C;T) |
Make rs41564218(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355488 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs41564218 |
dbSNP (classic) | rs41564218 |
ClinGen | rs41564218 |
ebi | rs41564218 |
HLI | rs41564218 |
Exac | rs41564218 |
Gnomad | rs41564218 |
Varsome | rs41564218 |
LitVar | rs41564218 |
Map | rs41564218 |
PheGenI | rs41564218 |
Biobank | rs41564218 |
1000 genomes | rs41564218 |
hgdp | rs41564218 |
ensembl | rs41564218 |
geneview | rs41564218 |
scholar | rs41564218 |
rs41564218 | |
pharmgkb | rs41564218 |
gwascentral | rs41564218 |
openSNP | rs41564218 |
23andMe | rs41564218 |
SNPshot | rs41564218 |
SNPdbe | rs41564218 |
MSV3d | rs41564218 |
GWAS Ctlg | rs41564218 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41564218(T;T) |
Alt | rs41564218(T;T) |
Reference | Rs41564218(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31323265G>A |
CLNSRC | |
CLNACC |