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rs16861326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16861326(A;A)
Make rs16861326(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position17967993
is asnp
is mentioned by
dbSNPrs16861326
ebirs16861326
HLIrs16861326
Exacrs16861326
Varsomers16861326
Maprs16861326
PheGenIrs16861326
hapmaprs16861326
1000 genomesrs16861326
hgdprs16861326
ensemblrs16861326
gopubmedrs16861326
geneviewrs16861326
scholarrs16861326
googlers16861326
pharmgkbrs16861326
gwascentralrs16861326
openSNPrs16861326
23andMers16861326
23andMe allrs16861326
SNP Nexus

SNPshotrs16861326
SNPdbers16861326
MSV3drs16861326
GWAS Ctlgrs16861326
GMAF0.02342
Max Magnitude0
? (A;A) (A;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 0.000002
Odds Ratio 17.85 [NR]