Have questions? Visit https://www.reddit.com/r/SNPedia

rs17044137

From SNPedia

Orientationplus
Stabilizedplus
Make rs17044137(A;A)
Make rs17044137(A;T)
Make rs17044137(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position111874141
is asnp
is mentioned by
dbSNPrs17044137
ebirs17044137
HLIrs17044137
Exacrs17044137
Varsomers17044137
Maprs17044137
PheGenIrs17044137
hapmaprs17044137
1000 genomesrs17044137
hgdprs17044137
ensemblrs17044137
gopubmedrs17044137
geneviewrs17044137
scholarrs17044137
googlers17044137
pharmgkbrs17044137
gwascentralrs17044137
openSNPrs17044137
23andMers17044137
23andMe allrs17044137
SNP Nexus

SNPshotrs17044137
SNPdbers17044137
MSV3drs17044137
GWAS Ctlgrs17044137
GMAF0.2392
Max Magnitude
? (A;A) (A;T) (T;T) 28
Rs17044137
PubMed [PMID 17463246]
Affy Probeset SNP_A-4271462
Affy Orientation same
On GW 5.0 1
Alleles A/B A/T
Ancestral T
Population NEU
Allele A
Case Freq.
Control Freq. 0.23
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.13
Disease Type II Diabetes (T2D)


rs17044137 increases susceptibility to Type II Diabetes 1.13 times for carriers of the A allele [PMID 17463246]



[PMID 18443202OA-icon.png] Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.


[PMID 20126254OA-icon.png] Rare variants create synthetic genome-wide associations.


GET Evidence
rs17044137
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.320312
summary