rs112094427
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs112094427(A;A) |
Make rs112094427(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943620 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs112094427 |
dbSNP (classic) | rs112094427 |
ClinGen | rs112094427 |
ebi | rs112094427 |
HLI | rs112094427 |
Exac | rs112094427 |
Gnomad | rs112094427 |
Varsome | rs112094427 |
LitVar | rs112094427 |
Map | rs112094427 |
PheGenI | rs112094427 |
Biobank | rs112094427 |
1000 genomes | rs112094427 |
hgdp | rs112094427 |
ensembl | rs112094427 |
geneview | rs112094427 |
scholar | rs112094427 |
rs112094427 | |
pharmgkb | rs112094427 |
gwascentral | rs112094427 |
openSNP | rs112094427 |
23andMe | rs112094427 |
SNPshot | rs112094427 |
SNPdbe | rs112094427 |
MSV3d | rs112094427 |
GWAS Ctlg | rs112094427 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs112094427(A;A) |
Alt | rs112094427(A;A) |
Reference | Rs112094427(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911397T>A |
CLNSRC | |
CLNACC |