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

rs587782228

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782228(A;A)
Make rs587782228(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45330557
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587782228
ebirs587782228
HLIrs587782228
Exacrs587782228
Varsomers587782228
Maprs587782228
PheGenIrs587782228
hapmaprs587782228
1000 genomesrs587782228
hgdprs587782228
ensemblrs587782228
gopubmedrs587782228
geneviewrs587782228
scholarrs587782228
googlers587782228
pharmgkbrs587782228
gwascentralrs587782228
openSNPrs587782228
23andMers587782228
23andMe allrs587782228
SNP Nexus

SNPshotrs587782228
SNPdbers587782228
MSV3drs587782228
GWAS Ctlgrs587782228
Max Magnitude0
ClinVar
Risk rs587782228(A,T;A,T)
Alt rs587782228(A,T;A,T)
Reference rs587782228(G;G)
Significance Probable-Pathogenic
Disease MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000001.10:g.45796229C>A; NC_000001.10:g.45796229C>T
CLNSRC
CLNACC RCV000204688.2, RCV000215469.1, RCV000130919.4, RCV000197197.1, RCV000212720.1,