rs2641348

minus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs2641348(C;C)

Make rs2641348(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

119895261

Gene

ADAM30

is a	snp
is	mentioned by
dbSNP	rs2641348
dbSNP (classic)	rs2641348
ClinGen	rs2641348
ebi	rs2641348
HLI	rs2641348
Exac	rs2641348
Gnomad	rs2641348
Varsome	rs2641348
LitVar	rs2641348
Map	rs2641348
PheGenI	rs2641348
Biobank	rs2641348
1000 genomes	rs2641348
hgdp	rs2641348
ensembl	rs2641348
geneview	rs2641348
scholar	rs2641348
google	rs2641348
pharmgkb	rs2641348
gwascentral	rs2641348
openSNP	rs2641348
23andMe	rs2641348
SNPshot	rs2641348
SNPdbe	rs2641348
MSV3d	rs2641348
GWAS Ctlg	rs2641348

GMAF

0.1543

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

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

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

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

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

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

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

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

[PMID 19956539 ] How many genetic variants remain to be discovered?