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rs587781338

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781338(C;T)
Make rs587781338(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332080
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587781338
ebirs587781338
HLIrs587781338
Exacrs587781338
Varsomers587781338
Maprs587781338
PheGenIrs587781338
hapmaprs587781338
1000 genomesrs587781338
hgdprs587781338
ensemblrs587781338
gopubmedrs587781338
geneviewrs587781338
scholarrs587781338
googlers587781338
pharmgkbrs587781338
gwascentralrs587781338
openSNPrs587781338
23andMers587781338
23andMe allrs587781338
SNP Nexus

SNPshotrs587781338
SNPdbers587781338
MSV3drs587781338
GWAS Ctlgrs587781338
Max Magnitude0
ClinVar
Risk rs587781338(T;T)
Alt rs587781338(T;T)
Reference rs587781338(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45797752G>A
CLNSRC
CLNACC RCV000129103.2,