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rs6545977

From SNPedia

Orientationplus
Stabilizedplus
Make rs6545977(A;A)
Make rs6545977(A;G)
Make rs6545977(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position63074029
is asnp
is mentioned by
dbSNPrs6545977
ebirs6545977
HLIrs6545977
Exacrs6545977
Varsomers6545977
Maprs6545977
PheGenIrs6545977
hapmaprs6545977
1000 genomesrs6545977
hgdprs6545977
ensemblrs6545977
gopubmedrs6545977
geneviewrs6545977
scholarrs6545977
googlers6545977
pharmgkbrs6545977
gwascentralrs6545977
openSNPrs6545977
23andMers6545977
23andMe allrs6545977
SNP Nexus

SNPshotrs6545977
SNPdbers6545977
MSV3drs6545977
GWAS Ctlgrs6545977
GMAF0.4293
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 5E-7
Odds Ratio NR NR


GET Evidence
rs6545977
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary