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rs6987702

From SNPedia

Orientationplus
Stabilizedplus
Make rs6987702(C;C)
Make rs6987702(C;T)
Make rs6987702(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position125492484
is asnp
is mentioned by
dbSNPrs6987702
ebirs6987702
HLIrs6987702
Exacrs6987702
Varsomers6987702
Maprs6987702
PheGenIrs6987702
hapmaprs6987702
1000 genomesrs6987702
hgdprs6987702
ensemblrs6987702
gopubmedrs6987702
geneviewrs6987702
scholarrs6987702
googlers6987702
pharmgkbrs6987702
gwascentralrs6987702
openSNPrs6987702
23andMers6987702
23andMe allrs6987702
SNP Nexus

SNPshotrs6987702
SNPdbers6987702
MSV3drs6987702
GWAS Ctlgrs6987702
GMAF0.4793
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19060911OA-icon.png]
Trait Cholesterol, total
Title Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Risk Allele G
P-val 3E-9
Odds Ratio 0.07 [NR] SD increase




GET Evidence
rs6987702
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484127
summary