rs2860580
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2860580(C;C) |
Make rs2860580(C;T) |
Make rs2860580(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29938914 |
Gene | HCG4P5 |
is a | snp |
is | mentioned by |
dbSNP | rs2860580 |
dbSNP (classic) | rs2860580 |
ClinGen | rs2860580 |
ebi | rs2860580 |
HLI | rs2860580 |
Exac | rs2860580 |
Gnomad | rs2860580 |
Varsome | rs2860580 |
LitVar | rs2860580 |
Map | rs2860580 |
PheGenI | rs2860580 |
Biobank | rs2860580 |
1000 genomes | rs2860580 |
hgdp | rs2860580 |
ensembl | rs2860580 |
geneview | rs2860580 |
scholar | rs2860580 |
rs2860580 | |
pharmgkb | rs2860580 |
gwascentral | rs2860580 |
openSNP | rs2860580 |
23andMe | rs2860580 |
SNPshot | rs2860580 |
SNPdbe | rs2860580 |
MSV3d | rs2860580 |
GWAS Ctlg | rs2860580 |
GMAF | 0.3802 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20512145] |
Trait | Nasopharyngeal carcinoma |
Title | A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. |
Risk Allele | |
P-val | 5E-67 |
Odds Ratio | 1.72 [1.61-1.82] |
[PMID 18519066] Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.
[PMID 27517745] Nasopharyngeal carcinoma risk prediction via salivary detection of host and Epstein-Barr virus genetic variants.