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rs445114

From SNPedia

Orientationplus
Stabilizedplus
Make rs445114(C;C)
Make rs445114(C;T)
Make rs445114(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127310936
GeneLOC101930033
is asnp
is mentioned by
dbSNPrs445114
ebirs445114
HLIrs445114
Exacrs445114
Varsomers445114
Maprs445114
PheGenIrs445114
hapmaprs445114
1000 genomesrs445114
hgdprs445114
ensemblrs445114
gopubmedrs445114
geneviewrs445114
scholarrs445114
googlers445114
pharmgkbrs445114
gwascentralrs445114
openSNPrs445114
23andMers445114
23andMe allrs445114
SNP Nexus

SNPshotrs445114
SNPdbers445114
MSV3drs445114
GWAS Ctlgrs445114
GMAF0.4596
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19767754OA-icon.png] Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
OMIM611100
Desc
Variant
Relatedalso
GWAS snp
PMID [PMID 21743057OA-icon.png]
Trait
Title Genome-wide association study identifies new prostate cancer susceptibility loci.
Risk Allele T
P-val 5E-7
Odds Ratio 1.2200 [1.12-1.32]


[PMID 20690139] Meta-analysis of genome-wide and replication association studies on prostate cancer.


GET Evidence
rs445114
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.444444
summary



[PMID 23159463] Genetic sequence variants are associated with severity of lower urinary tract symptoms and prostate cancer susceptibility.


[PMID 26248686] Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy