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rs876660787

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 3 Carrier of a MUTYH-related familial adenomatous polyposis mutation
Make rs876660787(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332959
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876660787
dbSNP (classic)rs876660787
ClinGenrs876660787
ebirs876660787
HLIrs876660787
Exacrs876660787
Gnomadrs876660787
Varsomers876660787
LitVarrs876660787
Maprs876660787
PheGenIrs876660787
Biobankrs876660787
1000 genomesrs876660787
hgdprs876660787
ensemblrs876660787
geneviewrs876660787
scholarrs876660787
googlers876660787
pharmgkbrs876660787
gwascentralrs876660787
openSNPrs876660787
23andMers876660787
SNPshotrs876660787
SNPdbers876660787
MSV3drs876660787
GWAS Ctlgrs876660787
Max Magnitude3
ClinVar
Risk rs876660787(T;T)
Alt rs876660787(T;T)
Reference Rs876660787(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000001.10:g.45798631T>A
CLNSRC
CLNACC RCV000216618.1, RCV000485126.1,