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rs267603153

From SNPedia

Orientationplus
Stabilizedplus
Make rs267603153(C;C)
Make rs267603153(C;T)
Make rs267603153(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position69087152
GeneTPCN2
is asnp
is mentioned by
dbSNPrs267603153
dbSNP (old)rs267603153
ClinGenrs267603153
ebirs267603153
HLIrs267603153
Exacrs267603153
Gnomadrs267603153
Varsomers267603153
Maprs267603153
PheGenIrs267603153
Biobankrs267603153
1000 genomesrs267603153
hgdprs267603153
ensemblrs267603153
gopubmedrs267603153
geneviewrs267603153
scholarrs267603153
googlers267603153
pharmgkbrs267603153
gwascentralrs267603153
openSNPrs267603153
23andMers267603153
23andMe allrs267603153
SNP Nexus

SNPshotrs267603153
SNPdbers267603153
MSV3drs267603153
GWAS Ctlgrs267603153
Max Magnitude

[PMID 26918892OA-icon.png] Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population.