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rs7048394

From SNPedia

Orientationplus
Make rs7048394(C;C)
Make rs7048394(C;T)
Make rs7048394(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position97843151
GenePTCSC2
is asnp
is mentioned by
dbSNPrs7048394
ebirs7048394
HLIrs7048394
Exacrs7048394
Varsomers7048394
Maprs7048394
PheGenIrs7048394
hapmaprs7048394
1000 genomesrs7048394
hgdprs7048394
ensemblrs7048394
gopubmedrs7048394
geneviewrs7048394
scholarrs7048394
googlers7048394
pharmgkbrs7048394
gwascentralrs7048394
openSNPrs7048394
23andMers7048394
23andMe allrs7048394
SNP Nexus

SNPshotrs7048394
SNPdbers7048394
MSV3drs7048394
GWAS Ctlgrs7048394
Max Magnitude
? (C;C) (C;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.