rs1485993
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1485993(C;C) |
Make rs1485993(C;T) |
Make rs1485993(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 69547646 |
is a | snp |
is | mentioned by |
dbSNP | rs1485993 |
dbSNP (classic) | rs1485993 |
ClinGen | rs1485993 |
ebi | rs1485993 |
HLI | rs1485993 |
Exac | rs1485993 |
Gnomad | rs1485993 |
Varsome | rs1485993 |
LitVar | rs1485993 |
Map | rs1485993 |
PheGenI | rs1485993 |
Biobank | rs1485993 |
1000 genomes | rs1485993 |
hgdp | rs1485993 |
ensembl | rs1485993 |
geneview | rs1485993 |
scholar | rs1485993 |
rs1485993 | |
pharmgkb | rs1485993 |
gwascentral | rs1485993 |
openSNP | rs1485993 |
23andMe | rs1485993 |
SNPshot | rs1485993 |
SNPdbe | rs1485993 |
MSV3d | rs1485993 |
GWAS Ctlg | rs1485993 |
GMAF | 0.3994 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23537197] Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population
[PMID 21983787] Genome-wide association study identifies three new melanoma susceptibility loci.