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rs1735151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1735151(C;T)
Make rs1735151(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position39751374
GeneIGSF5
is asnp
is mentioned by
dbSNPrs1735151
ebirs1735151
HLIrs1735151
Exacrs1735151
Varsomers1735151
Maprs1735151
PheGenIrs1735151
hapmaprs1735151
1000 genomesrs1735151
hgdprs1735151
ensemblrs1735151
gopubmedrs1735151
geneviewrs1735151
scholarrs1735151
googlers1735151
pharmgkbrs1735151
gwascentralrs1735151
openSNPrs1735151
23andMers1735151
23andMe allrs1735151
SNP Nexus

SNPshotrs1735151
SNPdbers1735151
MSV3drs1735151
GWAS Ctlgrs1735151
GMAF0.3269
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele T
P-val 0.000009
Odds Ratio 1.1600 [1.09-1.24]