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rs10489087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10489087(A;A)
Make rs10489087(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position13792792
GeneLINC01182
is asnp
is mentioned by
dbSNPrs10489087
ebirs10489087
HLIrs10489087
Exacrs10489087
Varsomers10489087
Maprs10489087
PheGenIrs10489087
hapmaprs10489087
1000 genomesrs10489087
hgdprs10489087
ensemblrs10489087
gopubmedrs10489087
geneviewrs10489087
scholarrs10489087
googlers10489087
pharmgkbrs10489087
gwascentralrs10489087
openSNPrs10489087
23andMers10489087
23andMe allrs10489087
SNP Nexus

SNPshotrs10489087
SNPdbers10489087
MSV3drs10489087
GWAS Ctlgrs10489087
GMAF0.1644
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903294OA-icon.png]
Trait Hemostatic factors and hematological phenotypes
Title Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
Risk Allele
P-val 0.0000050000000000000004
Odds Ratio NR NR


GET Evidence
rs10489087
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary