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rs587782885

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782885(C;T)
Make rs587782885(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332440
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587782885
ebirs587782885
HLIrs587782885
Exacrs587782885
Varsomers587782885
Maprs587782885
PheGenIrs587782885
hapmaprs587782885
1000 genomesrs587782885
hgdprs587782885
ensemblrs587782885
gopubmedrs587782885
geneviewrs587782885
scholarrs587782885
googlers587782885
pharmgkbrs587782885
gwascentralrs587782885
openSNPrs587782885
23andMers587782885
23andMe allrs587782885
SNP Nexus

SNPshotrs587782885
SNPdbers587782885
MSV3drs587782885
GWAS Ctlgrs587782885
Max Magnitude0
ClinVar
Risk rs587782885(T;T)
Alt rs587782885(T;T)
Reference rs587782885(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Carcinoma of colon not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome Carcinoma of colon not provided
Reversed 1
HGVS NC_000001.10:g.45798112G>A
CLNSRC
CLNACC RCV000132522.2, RCV000144630.1, RCV000236829.1,