rs144480582
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs144480582(A;A) |
Make rs144480582(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 15768540 |
Gene | FBLIM1 |
is a | snp |
is | mentioned by |
dbSNP | rs144480582 |
dbSNP (classic) | rs144480582 |
ClinGen | rs144480582 |
ebi | rs144480582 |
HLI | rs144480582 |
Exac | rs144480582 |
Gnomad | rs144480582 |
Varsome | rs144480582 |
LitVar | rs144480582 |
Map | rs144480582 |
PheGenI | rs144480582 |
Biobank | rs144480582 |
1000 genomes | rs144480582 |
hgdp | rs144480582 |
ensembl | rs144480582 |
geneview | rs144480582 |
scholar | rs144480582 |
rs144480582 | |
pharmgkb | rs144480582 |
gwascentral | rs144480582 |
openSNP | rs144480582 |
23andMe | rs144480582 |
SNPshot | rs144480582 |
SNPdbe | rs144480582 |
MSV3d | rs144480582 |
GWAS Ctlg | rs144480582 |
Max Magnitude | 0 |
[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
ClinVar | |
---|---|
Risk | rs144480582(A;A) |
Alt | rs144480582(A;A) |
Reference | Rs144480582(G;G) |
Significance | Untested |
Disease | Malignant melanoma |
Variation | info |
Gene | FBLIM1 |
CLNDBN | Malignant melanoma |
Reversed | 0 |
HGVS | NC_000001.11:g.15768540G>A |
CLNSRC | ClinVar |
CLNACC | RCV000059967.2, |