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rs587781704

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781704(-;-)
Make rs587781704(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45334457
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587781704
ebirs587781704
HLIrs587781704
Exacrs587781704
Varsomers587781704
Maprs587781704
PheGenIrs587781704
hapmaprs587781704
1000 genomesrs587781704
hgdprs587781704
ensemblrs587781704
gopubmedrs587781704
geneviewrs587781704
scholarrs587781704
googlers587781704
pharmgkbrs587781704
gwascentralrs587781704
openSNPrs587781704
23andMers587781704
23andMe allrs587781704
SNP Nexus

SNPshotrs587781704
SNPdbers587781704
MSV3drs587781704
GWAS Ctlgrs587781704
Max Magnitude0
ClinVar
Risk rs587781704(;)
Alt rs587781704(;)
Reference rs587781704(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.45800129delC
CLNSRC
CLNACC RCV000129874.2,