rs144045930
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs144045930(C;T) |
Make rs144045930(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 33068660 |
Gene | HLA-DPA1 |
is a | snp |
is | mentioned by |
dbSNP | rs144045930 |
dbSNP (classic) | rs144045930 |
ClinGen | rs144045930 |
ebi | rs144045930 |
HLI | rs144045930 |
Exac | rs144045930 |
Gnomad | rs144045930 |
Varsome | rs144045930 |
LitVar | rs144045930 |
Map | rs144045930 |
PheGenI | rs144045930 |
Biobank | rs144045930 |
1000 genomes | rs144045930 |
hgdp | rs144045930 |
ensembl | rs144045930 |
geneview | rs144045930 |
scholar | rs144045930 |
rs144045930 | |
pharmgkb | rs144045930 |
gwascentral | rs144045930 |
openSNP | rs144045930 |
23andMe | rs144045930 |
SNPshot | rs144045930 |
SNPdbe | rs144045930 |
MSV3d | rs144045930 |
GWAS Ctlg | rs144045930 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs144045930(T;T) |
Alt | rs144045930(T;T) |
Reference | Rs144045930(C;C) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | HLA-DPA1 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000006.12:g.33068660C>T |
CLNSRC | ClinVar |
CLNACC | RCV000061404.2, |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.