rs41559921
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41559921(C;G) |
Make rs41559921(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356926 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs41559921 |
dbSNP (classic) | rs41559921 |
ClinGen | rs41559921 |
ebi | rs41559921 |
HLI | rs41559921 |
Exac | rs41559921 |
Gnomad | rs41559921 |
Varsome | rs41559921 |
LitVar | rs41559921 |
Map | rs41559921 |
PheGenI | rs41559921 |
Biobank | rs41559921 |
1000 genomes | rs41559921 |
hgdp | rs41559921 |
ensembl | rs41559921 |
geneview | rs41559921 |
scholar | rs41559921 |
rs41559921 | |
pharmgkb | rs41559921 |
gwascentral | rs41559921 |
openSNP | rs41559921 |
23andMe | rs41559921 |
SNPshot | rs41559921 |
SNPdbe | rs41559921 |
MSV3d | rs41559921 |
GWAS Ctlg | rs41559921 |
GMAF | 0.03398 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41559921(G;G) rs41559921(T;T) |
Alt | rs41559921(G;G) rs41559921(T;T) |
Reference | Rs41559921(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324703G>A; NC_000006.11:g.31324703G>C |
CLNSRC | |
CLNACC |