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rs2390582

From SNPedia

Orientationplus
Stabilizedplus
Make rs2390582(A;A)
Make rs2390582(A;G)
Make rs2390582(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position90478350
is asnp
is mentioned by
dbSNPrs2390582
ebirs2390582
HLIrs2390582
Exacrs2390582
Varsomers2390582
Maprs2390582
PheGenIrs2390582
hapmaprs2390582
1000 genomesrs2390582
hgdprs2390582
ensemblrs2390582
gopubmedrs2390582
geneviewrs2390582
scholarrs2390582
googlers2390582
pharmgkbrs2390582
gwascentralrs2390582
openSNPrs2390582
23andMers2390582
23andMe allrs2390582
SNP Nexus

SNPshotrs2390582
SNPdbers2390582
MSV3drs2390582
GWAS Ctlgrs2390582
GMAF0.2011
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs2390582
PubMedID [PMID 17903303OA-icon.png]
Condition Coronary artery calcification
Gene Intergenic
Risk Allele
pValue 1.00E-006
OR NA
95% CI



[PMID 17903293OA-icon.png] Genome-wide association with select biomarker traits in the Framingham Heart Study.


GET Evidence
rs2390582
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary