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rs5965182

From SNPedia

Orientationplus
Stabilizedplus
Make rs5965182(A;A)
Make rs5965182(A;T)
Make rs5965182(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position66386851
is asnp
is mentioned by
dbSNPrs5965182
ebirs5965182
HLIrs5965182
Exacrs5965182
Varsomers5965182
Maprs5965182
PheGenIrs5965182
hapmaprs5965182
1000 genomesrs5965182
hgdprs5965182
ensemblrs5965182
gopubmedrs5965182
geneviewrs5965182
scholarrs5965182
googlers5965182
pharmgkbrs5965182
gwascentralrs5965182
openSNPrs5965182
23andMers5965182
23andMe allrs5965182
SNP Nexus

SNPshotrs5965182
SNPdbers5965182
MSV3drs5965182
GWAS Ctlgrs5965182
GMAF0.208
Max Magnitude
? (A;A) (A;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 0.000006
Odds Ratio 11.73 [NR]