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rs587778536

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778536(-;-)
Make rs587778536(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45331700
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587778536
ebirs587778536
HLIrs587778536
Exacrs587778536
Varsomers587778536
Maprs587778536
PheGenIrs587778536
hapmaprs587778536
1000 genomesrs587778536
hgdprs587778536
ensemblrs587778536
gopubmedrs587778536
geneviewrs587778536
scholarrs587778536
googlers587778536
pharmgkbrs587778536
gwascentralrs587778536
openSNPrs587778536
23andMers587778536
23andMe allrs587778536
SNP Nexus

SNPshotrs587778536
SNPdbers587778536
MSV3drs587778536
GWAS Ctlgrs587778536
Max Magnitude0
ClinVar
Risk rs587778536(;)
Alt rs587778536(;)
Reference rs587778536(C;C)
Significance Pathogenic
Disease not specified Carcinoma of colon Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided
Variation info
Gene MUTYH
CLNDBN not specified Carcinoma of colon Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided
Reversed 1
HGVS NC_000001.10:g.45797372delG
CLNSRC
CLNACC RCV000121593.1, RCV000144632.1, RCV000164291.1, RCV000196379.3, RCV000235584.1,