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rs587781628

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781628(A;G)
Make rs587781628(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45331558
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587781628
ebirs587781628
HLIrs587781628
Exacrs587781628
Varsomers587781628
Maprs587781628
PheGenIrs587781628
hapmaprs587781628
1000 genomesrs587781628
hgdprs587781628
ensemblrs587781628
gopubmedrs587781628
geneviewrs587781628
scholarrs587781628
googlers587781628
pharmgkbrs587781628
gwascentralrs587781628
openSNPrs587781628
23andMers587781628
23andMe allrs587781628
SNP Nexus

SNPshotrs587781628
SNPdbers587781628
MSV3drs587781628
GWAS Ctlgrs587781628
Max Magnitude0
ClinVar
Risk rs587781628(G;G)
Alt rs587781628(G;G)
Reference rs587781628(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Carcinoma of colon
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome Carcinoma of colon
Reversed 1
HGVS NC_000001.10:g.45797230T>C
CLNSRC
CLNACC RCV000129730.2, RCV000172819.1,