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rs12518099

From SNPedia

Orientationplus
Stabilizedplus
Make rs12518099(A;A)
Make rs12518099(A;G)
Make rs12518099(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position90250292
GeneLINC01339
is asnp
is mentioned by
dbSNPrs12518099
ebirs12518099
HLIrs12518099
Exacrs12518099
Varsomers12518099
Maprs12518099
PheGenIrs12518099
hapmaprs12518099
1000 genomesrs12518099
hgdprs12518099
ensemblrs12518099
gopubmedrs12518099
geneviewrs12518099
scholarrs12518099
googlers12518099
pharmgkbrs12518099
gwascentralrs12518099
openSNPrs12518099
23andMers12518099
23andMe allrs12518099
SNP Nexus

SNPshotrs12518099
SNPdbers12518099
MSV3drs12518099
GWAS Ctlgrs12518099
GMAF0.2934
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19734900]
Trait Type 2 diabetes and other traits
Title Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
Risk Allele C
P-val 7E-7
Odds Ratio 1.16 [1.10-1.22]

[PMID 22237986OA-icon.png] Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry.


GET Evidence
rs12518099
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary