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rs2641348

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2641348(C;C)
Make rs2641348(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position119895261
GeneADAM30
is asnp
is mentioned by
dbSNPrs2641348
dbSNP (classic)rs2641348
ClinGenrs2641348
ebirs2641348
HLIrs2641348
Exacrs2641348
Gnomadrs2641348
Varsomers2641348
LitVarrs2641348
Maprs2641348
PheGenIrs2641348
Biobankrs2641348
1000 genomesrs2641348
hgdprs2641348
ensemblrs2641348
geneviewrs2641348
scholarrs2641348
googlers2641348
pharmgkbrs2641348
gwascentralrs2641348
openSNPrs2641348
23andMers2641348
SNPshotrs2641348
SNPdbers2641348
MSV3drs2641348
GWAS Ctlgrs2641348
GMAF0.1543
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22052079OA-icon.png] Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs


[PMID 18372903OA-icon.png] Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.


[PMID 18591388OA-icon.png] Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk.


[PMID 18714373OA-icon.png] Novel meta-analysis-derived type 2 diabetes risk loci do not determine prediabetic phenotypes.


[PMID 19341491OA-icon.png] Genome-based prediction of common diseases: methodological considerations for future research.


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


[PMID 19862325OA-icon.png] PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population.


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