rs141132227
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141132227(C;T) |
Make rs141132227(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32814359 |
Gene | HLA-DOB |
is a | snp |
is | mentioned by |
dbSNP | rs141132227 |
dbSNP (classic) | rs141132227 |
ClinGen | rs141132227 |
ebi | rs141132227 |
HLI | rs141132227 |
Exac | rs141132227 |
Gnomad | rs141132227 |
Varsome | rs141132227 |
LitVar | rs141132227 |
Map | rs141132227 |
PheGenI | rs141132227 |
Biobank | rs141132227 |
1000 genomes | rs141132227 |
hgdp | rs141132227 |
ensembl | rs141132227 |
geneview | rs141132227 |
scholar | rs141132227 |
rs141132227 | |
pharmgkb | rs141132227 |
gwascentral | rs141132227 |
openSNP | rs141132227 |
23andMe | rs141132227 |
SNPshot | rs141132227 |
SNPdbe | rs141132227 |
MSV3d | rs141132227 |
GWAS Ctlg | rs141132227 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141132227(T;T) |
Alt | rs141132227(T;T) |
Reference | Rs141132227(C;C) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | HLA-DOB |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000006.12:g.32814359C>T |
CLNSRC | ClinVar |
CLNACC | RCV000061401.2, |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.