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rs10506458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10506458(A;A)
Make rs10506458(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position63051312
is asnp
is mentioned by
dbSNPrs10506458
ebirs10506458
HLIrs10506458
Exacrs10506458
Varsomers10506458
Maprs10506458
PheGenIrs10506458
hapmaprs10506458
1000 genomesrs10506458
hgdprs10506458
ensemblrs10506458
gopubmedrs10506458
geneviewrs10506458
scholarrs10506458
googlers10506458
pharmgkbrs10506458
gwascentralrs10506458
openSNPrs10506458
23andMers10506458
23andMe allrs10506458
SNP Nexus

SNPshotrs10506458
SNPdbers10506458
MSV3drs10506458
GWAS Ctlgrs10506458
GMAF0.1116
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
rs10506458
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
summary