Have questions? Visit https://www.reddit.com/r/SNPedia

rs587780088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780088(C;T)
Make rs587780088(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45334493
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587780088
dbSNP (old)rs587780088
ClinGenrs587780088
ebirs587780088
HLIrs587780088
Exacrs587780088
Varsomers587780088
Maprs587780088
PheGenIrs587780088
Biobankrs587780088
1000 genomesrs587780088
hgdprs587780088
ensemblrs587780088
gopubmedrs587780088
geneviewrs587780088
scholarrs587780088
googlers587780088
pharmgkbrs587780088
gwascentralrs587780088
openSNPrs587780088
23andMers587780088
23andMe allrs587780088
SNP Nexus

SNPshotrs587780088
SNPdbers587780088
MSV3drs587780088
GWAS Ctlgrs587780088
Max Magnitude0
ClinVar
Risk rs587780088(G;G) rs587780088(T;T)
Alt rs587780088(G;G) rs587780088(T;T)
Reference Rs587780088(C;C)
Significance Pathogenic
Disease not provided Carcinoma of colon MYH-associated polyposis Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN not provided Carcinoma of colon MYH-associated polyposis Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45800165G>A; NC_000001.10:g.45800165G>C
CLNSRC
CLNACC RCV000115767.2, RCV000144639.1, RCV000206117.3, RCV000447652.1, RCV000467752.1,