rs1050368
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1050368(A;A) |
Make rs1050368(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356301 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs1050368 |
dbSNP (classic) | rs1050368 |
ClinGen | rs1050368 |
ebi | rs1050368 |
HLI | rs1050368 |
Exac | rs1050368 |
Gnomad | rs1050368 |
Varsome | rs1050368 |
LitVar | rs1050368 |
Map | rs1050368 |
PheGenI | rs1050368 |
Biobank | rs1050368 |
1000 genomes | rs1050368 |
hgdp | rs1050368 |
ensembl | rs1050368 |
geneview | rs1050368 |
scholar | rs1050368 |
rs1050368 | |
pharmgkb | rs1050368 |
gwascentral | rs1050368 |
openSNP | rs1050368 |
23andMe | rs1050368 |
SNPshot | rs1050368 |
SNPdbe | rs1050368 |
MSV3d | rs1050368 |
GWAS Ctlg | rs1050368 |
GMAF | 0.03994 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1050368(A;A) rs1050368(G;G) |
Alt | rs1050368(A;A) rs1050368(G;G) |
Reference | Rs1050368(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324078G>T |
CLNSRC | |
CLNACC |