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rs34126013

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34126013(C;T)
Make rs34126013(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332458
GeneMUTYH
is asnp
is mentioned by
dbSNPrs34126013
ebirs34126013
HLIrs34126013
Exacrs34126013
Varsomers34126013
Maprs34126013
PheGenIrs34126013
hapmaprs34126013
1000 genomesrs34126013
hgdprs34126013
ensemblrs34126013
gopubmedrs34126013
geneviewrs34126013
scholarrs34126013
googlers34126013
pharmgkbrs34126013
gwascentralrs34126013
openSNPrs34126013
23andMers34126013
23andMe allrs34126013
SNP Nexus

SNPshotrs34126013
SNPdbers34126013
MSV3drs34126013
GWAS Ctlgrs34126013
Max Magnitude0
ClinVar
Risk rs34126013(T;T)
Alt rs34126013(T;T)
Reference rs34126013(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000001.10:g.45798130G>A
CLNSRC
CLNACC RCV000164664.1, RCV000235834.1,