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rs894673

From SNPedia

Orientationplus
Make rs894673(A;A)
Make rs894673(A;T)
Make rs894673(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position97849988
GenePTCSC2
is asnp
is mentioned by
dbSNPrs894673
ebirs894673
HLIrs894673
Exacrs894673
Varsomers894673
Maprs894673
PheGenIrs894673
hapmaprs894673
1000 genomesrs894673
hgdprs894673
ensemblrs894673
gopubmedrs894673
geneviewrs894673
scholarrs894673
googlers894673
pharmgkbrs894673
gwascentralrs894673
openSNPrs894673
23andMers894673
23andMe allrs894673
SNP Nexus

SNPshotrs894673
SNPdbers894673
MSV3drs894673
GWAS Ctlgrs894673
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 26843521] A comprehensive meta-analysis of case-control association studies to evaluate polymorphisms associated with the risk of differentiated thyroid carcinoma.