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rs587780078

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780078(-;-)
Make rs587780078(-;GG)
Make rs587780078(GG;GG)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45331514
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587780078
ebirs587780078
HLIrs587780078
Exacrs587780078
Varsomers587780078
Maprs587780078
PheGenIrs587780078
hapmaprs587780078
1000 genomesrs587780078
hgdprs587780078
ensemblrs587780078
gopubmedrs587780078
geneviewrs587780078
scholarrs587780078
googlers587780078
pharmgkbrs587780078
gwascentralrs587780078
openSNPrs587780078
23andMers587780078
23andMe allrs587780078
SNP Nexus

SNPshotrs587780078
SNPdbers587780078
MSV3drs587780078
GWAS Ctlgrs587780078
Max Magnitude0
ClinVar
Risk rs587780078(GG;GG)
Alt rs587780078(GG;GG)
Reference rs587780078(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Carcinoma of colon MYH-associated polyposis not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome Carcinoma of colon MYH-associated polyposis not provided
Reversed 1
HGVS NC_000001.10:g.45797187_45797188dupCC
CLNSRC
CLNACC RCV000115749.5, RCV000144636.1, RCV000191935.3, RCV000235187.1,