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rs583012

From SNPedia

Orientationplus
Stabilizedplus
Make rs583012(A;A)
Make rs583012(A;G)
Make rs583012(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position53535114
is asnp
is mentioned by
dbSNPrs583012
ebirs583012
HLIrs583012
Exacrs583012
Varsomers583012
Maprs583012
PheGenIrs583012
hapmaprs583012
1000 genomesrs583012
hgdprs583012
ensemblrs583012
gopubmedrs583012
geneviewrs583012
scholarrs583012
googlers583012
pharmgkbrs583012
gwascentralrs583012
openSNPrs583012
23andMers583012
23andMe allrs583012
SNP Nexus

SNPshotrs583012
SNPdbers583012
MSV3drs583012
GWAS Ctlgrs583012
GMAF0.1635
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 0.0000019999999999999999
Odds Ratio NR NR

[PMID 17903293OA-icon.png] select biomarker trait being C-reactive protein (CRP) levels


GET Evidence
rs583012
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.765625
summary