Have questions? Visit https://www.reddit.com/r/SNPedia

rs1327301

From SNPedia

Orientationplus
Stabilizedplus
Make rs1327301(C;C)
Make rs1327301(C;T)
Make rs1327301(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position51467205
is asnp
is mentioned by
dbSNPrs1327301
ebirs1327301
HLIrs1327301
Exacrs1327301
Varsomers1327301
Maprs1327301
PheGenIrs1327301
hapmaprs1327301
1000 genomesrs1327301
hgdprs1327301
ensemblrs1327301
gopubmedrs1327301
geneviewrs1327301
scholarrs1327301
googlers1327301
pharmgkbrs1327301
gwascentralrs1327301
openSNPrs1327301
23andMers1327301
23andMe allrs1327301
SNP Nexus

SNPshotrs1327301
SNPdbers1327301
MSV3drs1327301
GWAS Ctlgrs1327301
GMAF0.2098
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19767753OA-icon.png]
Trait Prostate cancer
Title Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Risk Allele T
P-val 2E-10
Odds Ratio NR NR


[PMID 19549809OA-icon.png] Fine-mapping and family-based association analyses of prostate cancer risk variants at Xp11.


GET Evidence
rs1327301
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.304348
summary