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rs587780749

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780749(G;T)
Make rs587780749(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332443
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587780749
ebirs587780749
HLIrs587780749
Exacrs587780749
Varsomers587780749
Maprs587780749
PheGenIrs587780749
hapmaprs587780749
1000 genomesrs587780749
hgdprs587780749
ensemblrs587780749
gopubmedrs587780749
geneviewrs587780749
scholarrs587780749
googlers587780749
pharmgkbrs587780749
gwascentralrs587780749
openSNPrs587780749
23andMers587780749
23andMe allrs587780749
SNP Nexus

SNPshotrs587780749
SNPdbers587780749
MSV3drs587780749
GWAS Ctlgrs587780749
Max Magnitude0
ClinVar
Risk rs587780749(A,T;A,T)
Alt rs587780749(A,T;A,T)
Reference rs587780749(G;G)
Significance Probable-Pathogenic
Disease MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.45798115C>A; NC_000001.10:g.45798115C>T
CLNSRC
CLNACC RCV000123154.1, RCV000131615.5, RCV000212707.1, RCV000222948.1,