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rs587782716

From SNPedia

Orientationminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs587782716(AG;AG)
Make rs587782716(AG;GC)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45329405
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587782716
ebirs587782716
HLIrs587782716
Exacrs587782716
Varsomers587782716
Maprs587782716
PheGenIrs587782716
hapmaprs587782716
1000 genomesrs587782716
hgdprs587782716
ensemblrs587782716
gopubmedrs587782716
geneviewrs587782716
scholarrs587782716
googlers587782716
pharmgkbrs587782716
gwascentralrs587782716
openSNPrs587782716
23andMers587782716
23andMe allrs587782716
SNP Nexus

SNPshotrs587782716
SNPdbers587782716
MSV3drs587782716
GWAS Ctlgrs587782716
Max Magnitude0
ClinVar
Risk rs587782716(AG;AG)
Alt rs587782716(AG;AG)
Reference rs587782716(GC;GC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45795077_45795078delGCinsCT
CLNSRC
CLNACC RCV000132196.2,