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rs9660710

From SNPedia

Orientationplus
Make rs9660710(A;A)
Make rs9660710(A;C)
Make rs9660710(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position1163962
is asnp
is mentioned by
dbSNPrs9660710
ebirs9660710
HLIrs9660710
Exacrs9660710
Varsomers9660710
Maprs9660710
PheGenIrs9660710
hapmaprs9660710
1000 genomesrs9660710
hgdprs9660710
ensemblrs9660710
gopubmedrs9660710
geneviewrs9660710
scholarrs9660710
googlers9660710
pharmgkbrs9660710
gwascentralrs9660710
openSNPrs9660710
23andMers9660710
23andMe allrs9660710
SNP Nexus

SNPshotrs9660710
SNPdbers9660710
MSV3drs9660710
GWAS Ctlgrs9660710
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 27374108] Genetic variants in regulatory regions of microRNAs are associated with lung cancer risk.