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rs6580742

From SNPedia

Orientationplus
Make rs6580742(C;C)
Make rs6580742(C;T)
Make rs6580742(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position50334028
GeneFAM186A
is asnp
is mentioned by
dbSNPrs6580742
ebirs6580742
HLIrs6580742
Exacrs6580742
Varsomers6580742
Maprs6580742
PheGenIrs6580742
hapmaprs6580742
1000 genomesrs6580742
hgdprs6580742
ensemblrs6580742
gopubmedrs6580742
geneviewrs6580742
scholarrs6580742
googlers6580742
pharmgkbrs6580742
gwascentralrs6580742
openSNPrs6580742
23andMers6580742
23andMe allrs6580742
SNP Nexus

SNPshotrs6580742
SNPdbers6580742
MSV3drs6580742
GWAS Ctlgrs6580742
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