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rs1359790

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1359790(C;T)
Make rs1359790(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position80143021
is asnp
is mentioned by
dbSNPrs1359790
ebirs1359790
HLIrs1359790
Exacrs1359790
Varsomers1359790
Maprs1359790
PheGenIrs1359790
hapmaprs1359790
1000 genomesrs1359790
hgdprs1359790
ensemblrs1359790
gopubmedrs1359790
geneviewrs1359790
scholarrs1359790
googlers1359790
pharmgkbrs1359790
gwascentralrs1359790
openSNPrs1359790
23andMers1359790
23andMe allrs1359790
SNP Nexus

SNPshotrs1359790
SNPdbers1359790
MSV3drs1359790
GWAS Ctlgrs1359790
GMAF0.2346
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20862305OA-icon.png]
Trait
Title Identification of new genetic risk variants for type 2 diabetes
Risk Allele G
P-val 6E-9
Odds Ratio 1.15 [1.10-1.20]


[PMID 21909839] Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population.

GWAS snp
PMID [PMID 24509480OA-icon.png]
Trait Type 2 diabetes
Title Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Risk Allele G
P-val 6E-6
Odds Ratio 1.10 [1.05-1.14]