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rs10877887

From SNPedia

Orientationplus
Stabilizedplus
Make rs10877887(C;C)
Make rs10877887(C;T)
Make rs10877887(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position62603400
GeneC12orf61, MIRLET7I
is asnp
is mentioned by
dbSNPrs10877887
ebirs10877887
HLIrs10877887
Exacrs10877887
Varsomers10877887
Maprs10877887
PheGenIrs10877887
hapmaprs10877887
1000 genomesrs10877887
hgdprs10877887
ensemblrs10877887
gopubmedrs10877887
geneviewrs10877887
scholarrs10877887
googlers10877887
pharmgkbrs10877887
gwascentralrs10877887
openSNPrs10877887
23andMers10877887
23andMe allrs10877887
SNP Nexus

SNPshotrs10877887
SNPdbers10877887
MSV3drs10877887
GWAS Ctlgrs10877887
GMAF0.405
Max Magnitude

[PMID 24103425] A potentially functional polymorphism in the promoter region of let-7 family is associated with survival of hepatocellular carcinoma

[PMID 26512603] Association Between Genetic Polymorphisms in the Promoter Regions of Let-7 and Risk of Papillary Thyroid Carcinoma: A Case-Control Study [PMID 26705209] A Potential Polymorphism in the Promoter of Let-7 is Associated With an Increased Risk of Intracranial Aneurysm: A Case-Control Study.