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rs6741148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6741148(G;G)
Make rs6741148(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position38050689
GeneRMDN2
is asnp
is mentioned by
dbSNPrs6741148
ebirs6741148
HLIrs6741148
Exacrs6741148
Varsomers6741148
Maprs6741148
PheGenIrs6741148
hapmaprs6741148
1000 genomesrs6741148
hgdprs6741148
ensemblrs6741148
gopubmedrs6741148
geneviewrs6741148
scholarrs6741148
googlers6741148
pharmgkbrs6741148
gwascentralrs6741148
openSNPrs6741148
23andMers6741148
23andMe allrs6741148
SNP Nexus

SNPshotrs6741148
SNPdbers6741148
MSV3drs6741148
GWAS Ctlgrs6741148
GMAF0.2489
Max Magnitude0
? (G;G) (G;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 0.000004
Odds Ratio 5.20 [NR]