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rs1129406

From SNPedia

Orientationplus
Make rs1129406(C;C)
Make rs1129406(C;T)
Make rs1129406(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position50809588
GeneATF1
is asnp
is mentioned by
dbSNPrs1129406
ebirs1129406
HLIrs1129406
Exacrs1129406
Varsomers1129406
Maprs1129406
PheGenIrs1129406
hapmaprs1129406
1000 genomesrs1129406
hgdprs1129406
ensemblrs1129406
gopubmedrs1129406
geneviewrs1129406
scholarrs1129406
googlers1129406
pharmgkbrs1129406
gwascentralrs1129406
openSNPrs1129406
23andMers1129406
23andMe allrs1129406
SNP Nexus

SNPshotrs1129406
SNPdbers1129406
MSV3drs1129406
GWAS Ctlgrs1129406
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26553438OA-icon.png] Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer