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rs4460176

From SNPedia

Orientationplus
Stabilizedplus
Make rs4460176(G;G)
Make rs4460176(G;T)
Make rs4460176(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position110161259
is asnp
is mentioned by
dbSNPrs4460176
ebirs4460176
HLIrs4460176
Exacrs4460176
Varsomers4460176
Maprs4460176
PheGenIrs4460176
hapmaprs4460176
1000 genomesrs4460176
hgdprs4460176
ensemblrs4460176
gopubmedrs4460176
geneviewrs4460176
scholarrs4460176
googlers4460176
pharmgkbrs4460176
gwascentralrs4460176
openSNPrs4460176
23andMers4460176
23andMe allrs4460176
SNP Nexus

SNPshotrs4460176
SNPdbers4460176
MSV3drs4460176
GWAS Ctlgrs4460176
GMAF0.4954
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs4460176
PubMedID [PMID 17903294OA-icon.png]
Condition Hemostatic factors and hematological phenotypes
Gene Intergenic
Risk Allele
pValue 3.00E-006
OR NA
95% CI



[PMID 17903299OA-icon.png] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.


GET Evidence
rs4460176
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507936
summary