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rs143353451

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143353451(A;A)
Make rs143353451(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332794
GeneMUTYH
is asnp
is mentioned by
dbSNPrs143353451
ebirs143353451
HLIrs143353451
Exacrs143353451
Varsomers143353451
Maprs143353451
PheGenIrs143353451
hapmaprs143353451
1000 genomesrs143353451
hgdprs143353451
ensemblrs143353451
gopubmedrs143353451
geneviewrs143353451
scholarrs143353451
googlers143353451
pharmgkbrs143353451
gwascentralrs143353451
openSNPrs143353451
23andMers143353451
23andMe allrs143353451
SNP Nexus

SNPshotrs143353451
SNPdbers143353451
MSV3drs143353451
GWAS Ctlgrs143353451
Max Magnitude0
ClinVar
Risk rs143353451(A,T;A,T)
Alt rs143353451(A,T;A,T)
Reference rs143353451(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000001.10:g.45798466C>A; NC_000001.10:g.45798466C>T
CLNSRC
CLNACC RCV000164867.1, RCV000160752.1, RCV000200700.1, RCV000214896.1,