rs17119461
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs17119461(C;C) |
Make rs17119461(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 105756594 |
Gene | LOC101927549 |
is a | snp |
is | mentioned by |
dbSNP | rs17119461 |
dbSNP (classic) | rs17119461 |
ClinGen | rs17119461 |
ebi | rs17119461 |
HLI | rs17119461 |
Exac | rs17119461 |
Gnomad | rs17119461 |
Varsome | rs17119461 |
LitVar | rs17119461 |
Map | rs17119461 |
PheGenI | rs17119461 |
Biobank | rs17119461 |
1000 genomes | rs17119461 |
hgdp | rs17119461 |
ensembl | rs17119461 |
geneview | rs17119461 |
scholar | rs17119461 |
rs17119461 | |
pharmgkb | rs17119461 |
gwascentral | rs17119461 |
openSNP | rs17119461 |
23andMe | rs17119461 |
SNPshot | rs17119461 |
SNPdbe | rs17119461 |
MSV3d | rs17119461 |
GWAS Ctlg | rs17119461 |
GMAF | 0.07117 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21706340] |
Trait | |
Title | A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. |
Risk Allele | |
P-val | 7E-12 |
Odds Ratio | 8.4000 [4.20-17.0] |