rs267603154
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs267603154(C;C) |
Make rs267603154(C;T) |
Make rs267603154(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 69087153 |
Gene | TPCN2 |
is a | snp |
is | mentioned by |
dbSNP | rs267603154 |
dbSNP (classic) | rs267603154 |
ClinGen | rs267603154 |
ebi | rs267603154 |
HLI | rs267603154 |
Exac | rs267603154 |
Gnomad | rs267603154 |
Varsome | rs267603154 |
LitVar | rs267603154 |
Map | rs267603154 |
PheGenI | rs267603154 |
Biobank | rs267603154 |
1000 genomes | rs267603154 |
hgdp | rs267603154 |
ensembl | rs267603154 |
geneview | rs267603154 |
scholar | rs267603154 |
rs267603154 | |
pharmgkb | rs267603154 |
gwascentral | rs267603154 |
openSNP | rs267603154 |
23andMe | rs267603154 |
SNPshot | rs267603154 |
SNPdbe | rs267603154 |
MSV3d | rs267603154 |
GWAS Ctlg | rs267603154 |
Max Magnitude | 0 |
[PMID 26918892] Genetic Variants of TPCN2 Associated with Type 2 Diabetes Risk in the Chinese Population.