Have questions? Visit https://www.reddit.com/r/SNPedia

rs7864322

From SNPedia

Orientationplus
Stabilizedplus
Make rs7864322(C;C)
Make rs7864322(C;T)
Make rs7864322(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position97786652
is asnp
is mentioned by
dbSNPrs7864322
ebirs7864322
HLIrs7864322
Exacrs7864322
Varsomers7864322
Maprs7864322
PheGenIrs7864322
hapmaprs7864322
1000 genomesrs7864322
hgdprs7864322
ensemblrs7864322
gopubmedrs7864322
geneviewrs7864322
scholarrs7864322
googlers7864322
pharmgkbrs7864322
gwascentralrs7864322
openSNPrs7864322
23andMers7864322
23andMe allrs7864322
SNP Nexus

SNPshotrs7864322
SNPdbers7864322
MSV3drs7864322
GWAS Ctlgrs7864322
Max Magnitude

[PMID 25918370OA-icon.png] Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer