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rs1875517

From SNPedia

Orientationminus
Stabilizedminus
Make rs1875517(C;C)
Make rs1875517(C;T)
Make rs1875517(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position117588720
is asnp
is mentioned by
dbSNPrs1875517
ebirs1875517
HLIrs1875517
Exacrs1875517
Varsomers1875517
Maprs1875517
PheGenIrs1875517
hapmaprs1875517
1000 genomesrs1875517
hgdprs1875517
ensemblrs1875517
gopubmedrs1875517
geneviewrs1875517
scholarrs1875517
googlers1875517
pharmgkbrs1875517
gwascentralrs1875517
openSNPrs1875517
23andMers1875517
23andMe allrs1875517
SNP Nexus

SNPshotrs1875517
SNPdbers1875517
MSV3drs1875517
GWAS Ctlgrs1875517
GMAF0.3903
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs1875517
PubMedID [PMID 17903300OA-icon.png]
Condition Waist circumference traits
Gene Intergenic
Risk Allele
pValue 2.00E-006
OR NA
95% CI



[PMID 17903303OA-icon.png] Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.


GET Evidence
rs1875517
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary