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rs11782652

From SNPedia

A 2013 GWAS study concluded that at the 8q21 locus, the strongest associated SNP with ovarian cancer was rs11782652, located in the first intron of the CHMP4C gene. rs11782652(G), with a frequency of 0.07 among European population, is the risk allele, with an OR of 1.19 (p<10e-9).[PMID 23535730OA-icon.png]


Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs11782652(A;G)
Make rs11782652(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position81741409
GeneCHMP4C
is asnp
is mentioned by
dbSNPrs11782652
dbSNP (old)rs11782652
ClinGenrs11782652
ebirs11782652
HLIrs11782652
Exacrs11782652
Varsomers11782652
Maprs11782652
PheGenIrs11782652
Biobankrs11782652
1000 genomesrs11782652
hgdprs11782652
ensemblrs11782652
gopubmedrs11782652
geneviewrs11782652
scholarrs11782652
googlers11782652
pharmgkbrs11782652
gwascentralrs11782652
openSNPrs11782652
23andMers11782652
23andMe allrs11782652
SNP Nexus

SNPshotrs11782652
SNPdbers11782652
MSV3drs11782652
GWAS Ctlgrs11782652
GMAF0.0528
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23535730OA-icon.png]
Trait Ovarian cancer
Title GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
Risk Allele G
P-val 6E-9
Odds Ratio 1.19 [1.12-1.26]