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rs12352658

From SNPedia

Orientationplus
Stabilizedplus
Make rs12352658(A;A)
Make rs12352658(A;G)
Make rs12352658(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position97789486
is asnp
is mentioned by
dbSNPrs12352658
ebirs12352658
HLIrs12352658
Exacrs12352658
Varsomers12352658
Maprs12352658
PheGenIrs12352658
hapmaprs12352658
1000 genomesrs12352658
hgdprs12352658
ensemblrs12352658
gopubmedrs12352658
geneviewrs12352658
scholarrs12352658
googlers12352658
pharmgkbrs12352658
gwascentralrs12352658
openSNPrs12352658
23andMers12352658
23andMe allrs12352658
SNP Nexus

SNPshotrs12352658
SNPdbers12352658
MSV3drs12352658
GWAS Ctlgrs12352658
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25918370OA-icon.png] Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer