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rs10484128

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10484128(A;A)
Make rs10484128(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position98176235
is asnp
is mentioned by
dbSNPrs10484128
ebirs10484128
HLIrs10484128
Exacrs10484128
Varsomers10484128
Maprs10484128
PheGenIrs10484128
hapmaprs10484128
1000 genomesrs10484128
hgdprs10484128
ensemblrs10484128
gopubmedrs10484128
geneviewrs10484128
scholarrs10484128
googlers10484128
pharmgkbrs10484128
gwascentralrs10484128
openSNPrs10484128
23andMers10484128
23andMe allrs10484128
SNP Nexus

SNPshotrs10484128
SNPdbers10484128
MSV3drs10484128
GWAS Ctlgrs10484128
GMAF0.07576
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 0.0000060000000000000002
Odds Ratio NR NR


GET Evidence
rs10484128
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary