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rs17036101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs17036101(A;A)
Make rs17036101(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12236345
is asnp
is mentioned by
dbSNPrs17036101
ebirs17036101
HLIrs17036101
Exacrs17036101
Varsomers17036101
Maprs17036101
PheGenIrs17036101
hapmaprs17036101
1000 genomesrs17036101
hgdprs17036101
ensemblrs17036101
gopubmedrs17036101
geneviewrs17036101
scholarrs17036101
googlers17036101
pharmgkbrs17036101
gwascentralrs17036101
openSNPrs17036101
23andMers17036101
23andMe allrs17036101
SNP Nexus

SNPshotrs17036101
SNPdbers17036101
MSV3drs17036101
GWAS Ctlgrs17036101
GMAF0.03444
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18372903OA-icon.png]
Trait Type 2 diabetes
Title Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Risk Allele G
P-val 1.9999999999999999E-7
Odds Ratio 1.15 [1.10-1.21]


[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


[PMID 19956539OA-icon.png] How many genetic variants remain to be discovered?


[PMID 20075150OA-icon.png] Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study.


[PMID 21084393OA-icon.png] Type 2 diabetes (T2D) associated polymorphisms regulate expression of adjacent transcripts in transformed lymphocytes, adipose, and muscle from Caucasian and African-American subjects.


[PMID 21278902OA-icon.png] Genetic risk profiling for prediction of type 2 diabetes.


GET Evidence
rs17036101
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.03125
summary