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rs587781295

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781295(A;A)
Make rs587781295(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45333166
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587781295
ebirs587781295
HLIrs587781295
Exacrs587781295
Varsomers587781295
Maprs587781295
PheGenIrs587781295
hapmaprs587781295
1000 genomesrs587781295
hgdprs587781295
ensemblrs587781295
gopubmedrs587781295
geneviewrs587781295
scholarrs587781295
googlers587781295
pharmgkbrs587781295
gwascentralrs587781295
openSNPrs587781295
23andMers587781295
23andMe allrs587781295
SNP Nexus

SNPshotrs587781295
SNPdbers587781295
MSV3drs587781295
GWAS Ctlgrs587781295
Max Magnitude0
ClinVar
Risk rs587781295(A;A)
Alt rs587781295(A;A)
Reference rs587781295(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.45798838C>T
CLNSRC
CLNACC RCV000128998.2,