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rs12770171

From SNPedia

Orientationminus
Stabilizedplus
Make rs12770171(C;C)
Make rs12770171(C;T)
Make rs12770171(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position46046508
GeneMSMB
is asnp
is mentioned by
dbSNPrs12770171
ebirs12770171
HLIrs12770171
Exacrs12770171
Varsomers12770171
Maprs12770171
PheGenIrs12770171
hapmaprs12770171
1000 genomesrs12770171
hgdprs12770171
ensemblrs12770171
gopubmedrs12770171
geneviewrs12770171
scholarrs12770171
googlers12770171
pharmgkbrs12770171
gwascentralrs12770171
openSNPrs12770171
23andMers12770171
23andMe allrs12770171
SNP Nexus

SNPshotrs12770171
SNPdbers12770171
MSV3drs12770171
GWAS Ctlgrs12770171
Max Magnitude

[PMID 24987558OA-icon.png] Promoter Polymorphism (rs12770170, -184C/T) of Microseminoprotein, Beta as a Risk Factor for Benign Prostatic Hyperplasia in Korean Population


[PMID 26240778OA-icon.png] The rs10993994 in the proximal MSMB promoter region is a functional polymorphism in Asian Indian subjects