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rs5971305

From SNPedia

Orientationplus
Stabilizedplus
Make rs5971305(A;A)
Make rs5971305(A;G)
Make rs5971305(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position28214936
is asnp
is mentioned by
dbSNPrs5971305
ebirs5971305
HLIrs5971305
Exacrs5971305
Varsomers5971305
Maprs5971305
PheGenIrs5971305
hapmaprs5971305
1000 genomesrs5971305
hgdprs5971305
ensemblrs5971305
gopubmedrs5971305
geneviewrs5971305
scholarrs5971305
googlers5971305
pharmgkbrs5971305
gwascentralrs5971305
openSNPrs5971305
23andMers5971305
23andMe allrs5971305
SNP Nexus

SNPshotrs5971305
SNPdbers5971305
MSV3drs5971305
GWAS Ctlgrs5971305
GMAF0.1892
Max Magnitude
? (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 0.000008
Odds Ratio 33.69 [NR]