rs113324237
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs113324237(G;T) |
Make rs113324237(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943635 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs113324237 |
dbSNP (classic) | rs113324237 |
ClinGen | rs113324237 |
ebi | rs113324237 |
HLI | rs113324237 |
Exac | rs113324237 |
Gnomad | rs113324237 |
Varsome | rs113324237 |
LitVar | rs113324237 |
Map | rs113324237 |
PheGenI | rs113324237 |
Biobank | rs113324237 |
1000 genomes | rs113324237 |
hgdp | rs113324237 |
ensembl | rs113324237 |
geneview | rs113324237 |
scholar | rs113324237 |
rs113324237 | |
pharmgkb | rs113324237 |
gwascentral | rs113324237 |
openSNP | rs113324237 |
23andMe | rs113324237 |
SNPshot | rs113324237 |
SNPdbe | rs113324237 |
MSV3d | rs113324237 |
GWAS Ctlg | rs113324237 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113324237(T;T) |
Alt | rs113324237(T;T) |
Reference | Rs113324237(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911412G>T |
CLNSRC | |
CLNACC |