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

rs2165738

From SNPedia

Orientationminus
Stabilizedminus
Make rs2165738(C;C)
Make rs2165738(C;G)
Make rs2165738(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position24469940
is asnp
is mentioned by
dbSNPrs2165738
ebirs2165738
HLIrs2165738
Exacrs2165738
Varsomers2165738
Maprs2165738
PheGenIrs2165738
hapmaprs2165738
1000 genomesrs2165738
hgdprs2165738
ensemblrs2165738
gopubmedrs2165738
geneviewrs2165738
scholarrs2165738
googlers2165738
pharmgkbrs2165738
gwascentralrs2165738
openSNPrs2165738
23andMers2165738
23andMe allrs2165738
SNP Nexus

SNPshotrs2165738
SNPdbers2165738
MSV3drs2165738
GWAS Ctlgrs2165738
GMAF0.4118
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18978792OA-icon.png]
Trait Type 1 diabetes
Title Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
Risk Allele C
P-val 0.000004
Odds Ratio 1.07 [1.01-1.13]




GET Evidence
rs2165738
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary