Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781337

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781337(A;A)
Make rs587781337(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45331660
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587781337
ebirs587781337
HLIrs587781337
Exacrs587781337
Varsomers587781337
Maprs587781337
PheGenIrs587781337
hapmaprs587781337
1000 genomesrs587781337
hgdprs587781337
ensemblrs587781337
gopubmedrs587781337
geneviewrs587781337
scholarrs587781337
googlers587781337
pharmgkbrs587781337
gwascentralrs587781337
openSNPrs587781337
23andMers587781337
23andMe allrs587781337
SNP Nexus

SNPshotrs587781337
SNPdbers587781337
MSV3drs587781337
GWAS Ctlgrs587781337
Max Magnitude0
ClinVar
Risk rs587781337(A;A)
Alt rs587781337(A;A)
Reference rs587781337(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45797332C>T
CLNSRC
CLNACC RCV000129098.2,