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

rs876660837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a MUTYH-related familial adenomatous polyposis mutation
Make rs876660837(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45331335
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876660837
dbSNP (classic)rs876660837
ClinGenrs876660837
ebirs876660837
HLIrs876660837
Exacrs876660837
Gnomadrs876660837
Varsomers876660837
LitVarrs876660837
Maprs876660837
PheGenIrs876660837
Biobankrs876660837
1000 genomesrs876660837
hgdprs876660837
ensemblrs876660837
geneviewrs876660837
scholarrs876660837
googlers876660837
pharmgkbrs876660837
gwascentralrs876660837
openSNPrs876660837
23andMers876660837
SNPshotrs876660837
SNPdbers876660837
MSV3drs876660837
GWAS Ctlgrs876660837
Max Magnitude3
ClinVar
Risk rs876660837(T;T)
Alt rs876660837(T;T)
Reference Rs876660837(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45797007C>A
CLNSRC
CLNACC RCV000218775.1,