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rs587780751

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780751(A;C)
Make rs587780751(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332163
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587780751
ebirs587780751
HLIrs587780751
Exacrs587780751
Varsomers587780751
Maprs587780751
PheGenIrs587780751
hapmaprs587780751
1000 genomesrs587780751
hgdprs587780751
ensemblrs587780751
gopubmedrs587780751
geneviewrs587780751
scholarrs587780751
googlers587780751
pharmgkbrs587780751
gwascentralrs587780751
openSNPrs587780751
23andMers587780751
23andMe allrs587780751
SNP Nexus

SNPshotrs587780751
SNPdbers587780751
MSV3drs587780751
GWAS Ctlgrs587780751
Max Magnitude0
ClinVar
Risk rs587780751(C;C)
Alt rs587780751(C;C)
Reference rs587780751(A;A)
Significance Pathogenic
Disease MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000001.10:g.45797835T>G
CLNSRC
CLNACC RCV000123158.4, RCV000129539.4, RCV000212711.1,