rs11423052
From SNPedia
Merged into | rs5875313 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs11423052(-;C) |
Make rs11423052(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355999 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs11423052 |
dbSNP (classic) | rs11423052 |
ClinGen | rs11423052 |
ebi | rs11423052 |
HLI | rs11423052 |
Exac | rs11423052 |
Gnomad | rs11423052 |
Varsome | rs11423052 |
LitVar | rs11423052 |
Map | rs11423052 |
PheGenI | rs11423052 |
Biobank | rs11423052 |
1000 genomes | rs11423052 |
hgdp | rs11423052 |
ensembl | rs11423052 |
geneview | rs11423052 |
scholar | rs11423052 |
rs11423052 | |
pharmgkb | rs11423052 |
gwascentral | rs11423052 |
openSNP | rs11423052 |
23andMe | rs11423052 |
SNPshot | rs11423052 |
SNPdbe | rs11423052 |
MSV3d | rs11423052 |
GWAS Ctlg | rs11423052 |
Status | Merged into rs5875313 |
GMAF | 0.2984 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs11423052(C;C) |
Alt | rs11423052(C;C) |
Reference | Rs11423052(;) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31323776_31323777insC |
CLNSRC | |
CLNACC |