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

rs10741243

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10741243(C;C)
Make rs10741243(C;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position131149699
GeneTCERG1L
is asnp
is mentioned by
dbSNPrs10741243
dbSNP (classic)rs10741243
ClinGenrs10741243
ebirs10741243
HLIrs10741243
Exacrs10741243
Gnomadrs10741243
Varsomers10741243
LitVarrs10741243
Maprs10741243
PheGenIrs10741243
Biobankrs10741243
1000 genomesrs10741243
hgdprs10741243
ensemblrs10741243
geneviewrs10741243
scholarrs10741243
googlers10741243
pharmgkbrs10741243
gwascentralrs10741243
openSNPrs10741243
23andMers10741243
SNPshotrs10741243
SNPdbers10741243
MSV3drs10741243
GWAS Ctlgrs10741243
GMAF0.1804
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 21490949OA-icon.png]
Trait
Title Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.
Risk Allele G
P-val 0.000005
Odds Ratio 1.7500 [1.38-2.23]