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rs10669586

From SNPedia

Orientationplus
Make rs10669586(-;-)
Make rs10669586(-;CT)
Make rs10669586(CT;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position46046600
GeneMSMB
is asnp
is mentioned by
dbSNPrs10669586
ebirs10669586
HLIrs10669586
Exacrs10669586
Varsomers10669586
Maprs10669586
PheGenIrs10669586
hapmaprs10669586
1000 genomesrs10669586
hgdprs10669586
ensemblrs10669586
gopubmedrs10669586
geneviewrs10669586
scholarrs10669586
googlers10669586
pharmgkbrs10669586
gwascentralrs10669586
openSNPrs10669586
23andMers10669586
23andMe allrs10669586
SNP Nexus

SNPshotrs10669586
SNPdbers10669586
MSV3drs10669586
GWAS Ctlgrs10669586
Max Magnitude

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