rs144003672
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs144003672(A;A) |
Make rs144003672(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 1309724 |
Gene | ACAP3, PUSL1 |
is a | snp |
is | mentioned by |
dbSNP | rs144003672 |
dbSNP (classic) | rs144003672 |
ClinGen | rs144003672 |
ebi | rs144003672 |
HLI | rs144003672 |
Exac | rs144003672 |
Gnomad | rs144003672 |
Varsome | rs144003672 |
LitVar | rs144003672 |
Map | rs144003672 |
PheGenI | rs144003672 |
Biobank | rs144003672 |
1000 genomes | rs144003672 |
hgdp | rs144003672 |
ensembl | rs144003672 |
geneview | rs144003672 |
scholar | rs144003672 |
rs144003672 | |
pharmgkb | rs144003672 |
gwascentral | rs144003672 |
openSNP | rs144003672 |
23andMe | rs144003672 |
SNPshot | rs144003672 |
SNPdbe | rs144003672 |
MSV3d | rs144003672 |
GWAS Ctlg | rs144003672 |
Max Magnitude | 0 |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
ClinVar | |
---|---|
Risk | rs144003672(A;A) |
Alt | rs144003672(A;A) |
Reference | Rs144003672(C;C) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | ACAP3 PUSL1 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000001.11:g.1309724C>A |
CLNSRC | ClinVar |
CLNACC | RCV000059856.2, |