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rs7847449

From SNPedia

Orientationplus
Stabilizedplus
Make rs7847449(A;A)
Make rs7847449(A;C)
Make rs7847449(C;C)
ReferenceGRCh38 38.1/142
Chromosome9
Position97789626
is asnp
is mentioned by
dbSNPrs7847449
ebirs7847449
HLIrs7847449
Exacrs7847449
Varsomers7847449
Maprs7847449
PheGenIrs7847449
hapmaprs7847449
1000 genomesrs7847449
hgdprs7847449
ensemblrs7847449
gopubmedrs7847449
geneviewrs7847449
scholarrs7847449
googlers7847449
pharmgkbrs7847449
gwascentralrs7847449
openSNPrs7847449
23andMers7847449
23andMe allrs7847449
SNP Nexus

SNPshotrs7847449
SNPdbers7847449
MSV3drs7847449
GWAS Ctlgrs7847449
Max Magnitude
? (A;A) (A;C) (C;C) 28

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