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rs2387326

From SNPedia

Orientationminus
Stabilizedminus
Make rs2387326(A;A)
Make rs2387326(A;G)
Make rs2387326(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position128135192
is asnp
is mentioned by
dbSNPrs2387326
ebirs2387326
HLIrs2387326
Exacrs2387326
Varsomers2387326
Maprs2387326
PheGenIrs2387326
hapmaprs2387326
1000 genomesrs2387326
hgdprs2387326
ensemblrs2387326
gopubmedrs2387326
geneviewrs2387326
scholarrs2387326
googlers2387326
pharmgkbrs2387326
gwascentralrs2387326
openSNPrs2387326
23andMers2387326
23andMe allrs2387326
SNP Nexus

SNPshotrs2387326
SNPdbers2387326
MSV3drs2387326
GWAS Ctlgrs2387326
GMAF0.2443
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR


GET Evidence
rs2387326
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary