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rs2716734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2716734(C;T)
Make rs2716734(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position39720581
is asnp
is mentioned by
dbSNPrs2716734
ebirs2716734
HLIrs2716734
Exacrs2716734
Varsomers2716734
Maprs2716734
PheGenIrs2716734
hapmaprs2716734
1000 genomesrs2716734
hgdprs2716734
ensemblrs2716734
gopubmedrs2716734
geneviewrs2716734
scholarrs2716734
googlers2716734
pharmgkbrs2716734
gwascentralrs2716734
openSNPrs2716734
23andMers2716734
23andMe allrs2716734
SNP Nexus

SNPshotrs2716734
SNPdbers2716734
MSV3drs2716734
GWAS Ctlgrs2716734
GMAF0.1015
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20932654OA-icon.png]
Trait
Title Genome-Wide Association Study to Identify Single Nucleotide Polymorphisms (SNPs) Associated With the Development of Erectile Dysfunction in African-American Men After Radiotherapy for Prostate Cancer
Risk Allele
P-val 0.000002
Odds Ratio 5.97 [NR]