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rs2806864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2806864(C;G)
Make rs2806864(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position116927159
GenePTGFRN
is asnp
is mentioned by
dbSNPrs2806864
ebirs2806864
HLIrs2806864
Exacrs2806864
Varsomers2806864
Maprs2806864
PheGenIrs2806864
hapmaprs2806864
1000 genomesrs2806864
hgdprs2806864
ensemblrs2806864
gopubmedrs2806864
geneviewrs2806864
scholarrs2806864
googlers2806864
pharmgkbrs2806864
gwascentralrs2806864
openSNPrs2806864
23andMers2806864
23andMe allrs2806864
SNP Nexus

SNPshotrs2806864
SNPdbers2806864
MSV3drs2806864
GWAS Ctlgrs2806864
GMAF0.1804
Max Magnitude0
? (C;C) (C;G) (G;G) 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 6E-7
Odds Ratio 6.42 [NR]