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rs587780082

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780082(C;T)
Make rs587780082(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45331835
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587780082
ebirs587780082
HLIrs587780082
Exacrs587780082
Varsomers587780082
Maprs587780082
PheGenIrs587780082
hapmaprs587780082
1000 genomesrs587780082
hgdprs587780082
ensemblrs587780082
gopubmedrs587780082
geneviewrs587780082
scholarrs587780082
googlers587780082
pharmgkbrs587780082
gwascentralrs587780082
openSNPrs587780082
23andMers587780082
23andMe allrs587780082
SNP Nexus

SNPshotrs587780082
SNPdbers587780082
MSV3drs587780082
GWAS Ctlgrs587780082
Max Magnitude0
ClinVar
Risk rs587780082(T;T)
Alt rs587780082(T;T)
Reference rs587780082(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.45797507G>A
CLNSRC
CLNACC RCV000115753.4, RCV000212713.1,