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rs10861905

From SNPedia

Orientationplus
Stabilizedplus
Make rs10861905(A;A)
Make rs10861905(A;C)
Make rs10861905(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position108373556
is asnp
is mentioned by
dbSNPrs10861905
ebirs10861905
HLIrs10861905
Exacrs10861905
Varsomers10861905
Maprs10861905
PheGenIrs10861905
hapmaprs10861905
1000 genomesrs10861905
hgdprs10861905
ensemblrs10861905
gopubmedrs10861905
geneviewrs10861905
scholarrs10861905
googlers10861905
pharmgkbrs10861905
gwascentralrs10861905
openSNPrs10861905
23andMers10861905
23andMe allrs10861905
SNP Nexus

SNPshotrs10861905
SNPdbers10861905
MSV3drs10861905
GWAS Ctlgrs10861905
GMAF0.1446
Max Magnitude
? (A;A) (A;C) (C;C) 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 8E-7
Odds Ratio 33.95 [NR]