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rs603446

From SNPedia

Orientationplus
Stabilizedplus
Make rs603446(C;C)
Make rs603446(C;T)
Make rs603446(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116783719
GeneZNF259
is asnp
is mentioned by
dbSNPrs603446
ebirs603446
HLIrs603446
Exacrs603446
Varsomers603446
Maprs603446
PheGenIrs603446
hapmaprs603446
1000 genomesrs603446
hgdprs603446
ensemblrs603446
gopubmedrs603446
geneviewrs603446
scholarrs603446
googlers603446
pharmgkbrs603446
gwascentralrs603446
openSNPrs603446
23andMers603446
23andMe allrs603446
SNP Nexus

SNPshotrs603446
SNPdbers603446
MSV3drs603446
GWAS Ctlgrs603446
GMAF0.3131
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21909109]
Trait
Title Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
Risk Allele T
P-val 2E-86
Odds Ratio 0.0876 [0.079-0.096] mg/dL decrease

[PMID 19047183OA-icon.png] GRM7 variants confer susceptibility to age-related hearing impairment.

[PMID 20017964OA-icon.png] Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood-ratio test and conditional score statistic.

[PMID 20018031OA-icon.png] The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study.