rs12770171
From SNPedia
Orientation | minus |
Stabilized | plus |
Make rs12770171(C;C) |
Make rs12770171(C;T) |
Make rs12770171(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 46046508 |
Gene | MSMB |
is a | snp |
is | mentioned by |
dbSNP | rs12770171 |
dbSNP (classic) | rs12770171 |
ClinGen | rs12770171 |
ebi | rs12770171 |
HLI | rs12770171 |
Exac | rs12770171 |
Gnomad | rs12770171 |
Varsome | rs12770171 |
LitVar | rs12770171 |
Map | rs12770171 |
PheGenI | rs12770171 |
Biobank | rs12770171 |
1000 genomes | rs12770171 |
hgdp | rs12770171 |
ensembl | rs12770171 |
geneview | rs12770171 |
scholar | rs12770171 |
rs12770171 | |
pharmgkb | rs12770171 |
gwascentral | rs12770171 |
openSNP | rs12770171 |
23andMe | rs12770171 |
SNPshot | rs12770171 |
SNPdbe | rs12770171 |
MSV3d | rs12770171 |
GWAS Ctlg | rs12770171 |
Max Magnitude | 0 |
[PMID 24987558] Promoter Polymorphism (rs12770170, -184C/T) of Microseminoprotein, Beta as a Risk Factor for Benign Prostatic Hyperplasia in Korean Population
[PMID 26240778] The rs10993994 in the proximal MSMB promoter region is a functional polymorphism in Asian Indian subjects