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rs140342925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140342925(C;T)
Make rs140342925(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position45332445
GeneMUTYH
is asnp
is mentioned by
dbSNPrs140342925
ebirs140342925
HLIrs140342925
Exacrs140342925
Varsomers140342925
Maprs140342925
PheGenIrs140342925
hapmaprs140342925
1000 genomesrs140342925
hgdprs140342925
ensemblrs140342925
gopubmedrs140342925
geneviewrs140342925
scholarrs140342925
googlers140342925
pharmgkbrs140342925
gwascentralrs140342925
openSNPrs140342925
23andMers140342925
23andMe allrs140342925
SNP Nexus

SNPshotrs140342925
SNPdbers140342925
MSV3drs140342925
GWAS Ctlgrs140342925
Max Magnitude0
ClinVar
Risk rs140342925(T;T)
Alt rs140342925(T;T)
Reference rs140342925(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided
Reversed 0
HGVS NC_000001.10:g.45798117C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000129105.4, RCV000196778.2, RCV000212706.1,