rs148699775
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148699775(A;A) |
Make rs148699775(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32581815 |
Gene | HLA-DRB1 |
is a | snp |
is | mentioned by |
dbSNP | rs148699775 |
dbSNP (classic) | rs148699775 |
ClinGen | rs148699775 |
ebi | rs148699775 |
HLI | rs148699775 |
Exac | rs148699775 |
Gnomad | rs148699775 |
Varsome | rs148699775 |
LitVar | rs148699775 |
Map | rs148699775 |
PheGenI | rs148699775 |
Biobank | rs148699775 |
1000 genomes | rs148699775 |
hgdp | rs148699775 |
ensembl | rs148699775 |
geneview | rs148699775 |
scholar | rs148699775 |
rs148699775 | |
pharmgkb | rs148699775 |
gwascentral | rs148699775 |
openSNP | rs148699775 |
23andMe | rs148699775 |
SNPshot | rs148699775 |
SNPdbe | rs148699775 |
MSV3d | rs148699775 |
GWAS Ctlg | rs148699775 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148699775(A;A) |
Alt | rs148699775(A;A) |
Reference | Rs148699775(G;G) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | LOC105369230 HLA-DRB1 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000006.12:g.32581815G>A |
CLNSRC | ClinVar |
CLNACC | RCV000061400.2, |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.