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rs1486139

From SNPedia

Orientationminus
Stabilizedminus
Make rs1486139(C;C)
Make rs1486139(C;T)
Make rs1486139(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position46236130
is asnp
is mentioned by
dbSNPrs1486139
ebirs1486139
HLIrs1486139
Exacrs1486139
Varsomers1486139
Maprs1486139
PheGenIrs1486139
hapmaprs1486139
1000 genomesrs1486139
hgdprs1486139
ensemblrs1486139
gopubmedrs1486139
geneviewrs1486139
scholarrs1486139
googlers1486139
pharmgkbrs1486139
gwascentralrs1486139
openSNPrs1486139
23andMers1486139
23andMe allrs1486139
SNP Nexus

SNPshotrs1486139
SNPdbers1486139
MSV3drs1486139
GWAS Ctlgrs1486139
GMAF0.4908
Max Magnitude
? (C;C) (C;T) (T;T) 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


GET Evidence
rs1486139
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary