rs112525507
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs112525507(A;A) |
Make rs112525507(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29945738 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs112525507 |
dbSNP (classic) | rs112525507 |
ClinGen | rs112525507 |
ebi | rs112525507 |
HLI | rs112525507 |
Exac | rs112525507 |
Gnomad | rs112525507 |
Varsome | rs112525507 |
LitVar | rs112525507 |
Map | rs112525507 |
PheGenI | rs112525507 |
Biobank | rs112525507 |
1000 genomes | rs112525507 |
hgdp | rs112525507 |
ensembl | rs112525507 |
geneview | rs112525507 |
scholar | rs112525507 |
rs112525507 | |
pharmgkb | rs112525507 |
gwascentral | rs112525507 |
openSNP | rs112525507 |
23andMe | rs112525507 |
SNPshot | rs112525507 |
SNPdbe | rs112525507 |
MSV3d | rs112525507 |
GWAS Ctlg | rs112525507 |
GMAF | 0.05877 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs112525507(A;A) |
Alt | rs112525507(A;A) |
Reference | Rs112525507(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.29913515C>T |
CLNSRC | |
CLNACC |