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rs4466137

From SNPedia

Orientationplus
Stabilizedplus
Make rs4466137(G;G)
Make rs4466137(G;T)
Make rs4466137(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position83689920
GeneHAPLN1
is asnp
is mentioned by
dbSNPrs4466137
ebirs4466137
HLIrs4466137
Exacrs4466137
Varsomers4466137
Maprs4466137
PheGenIrs4466137
hapmaprs4466137
1000 genomesrs4466137
hgdprs4466137
ensemblrs4466137
gopubmedrs4466137
geneviewrs4466137
scholarrs4466137
googlers4466137
pharmgkbrs4466137
gwascentralrs4466137
openSNPrs4466137
23andMers4466137
23andMe allrs4466137
SNP Nexus

SNPshotrs4466137
SNPdbers4466137
MSV3drs4466137
GWAS Ctlgrs4466137
GMAF0.2121
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs4466137
PubMedID [PMID 17903305OA-icon.png]
Condition Prostate cancer
Gene HAPLN1
Risk Allele
pValue 3.00E-006
OR NA
95% CI



GET Evidence
rs4466137
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.726562
summary