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rs13293512

From SNPedia

Orientationplus
Stabilizedplus
Make rs13293512(C;C)
Make rs13293512(C;T)
Make rs13293512(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position94167461
is asnp
is mentioned by
dbSNPrs13293512
ebirs13293512
HLIrs13293512
Exacrs13293512
Varsomers13293512
Maprs13293512
PheGenIrs13293512
hapmaprs13293512
1000 genomesrs13293512
hgdprs13293512
ensemblrs13293512
gopubmedrs13293512
geneviewrs13293512
scholarrs13293512
googlers13293512
pharmgkbrs13293512
gwascentralrs13293512
openSNPrs13293512
23andMers13293512
23andMe allrs13293512
SNP Nexus

SNPshotrs13293512
SNPdbers13293512
MSV3drs13293512
GWAS Ctlgrs13293512
GMAF0.2594
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.