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rs876660787

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660787(A;T)
Make rs876660787(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332959
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876660787
ebirs876660787
HLIrs876660787
Exacrs876660787
Varsomers876660787
Maprs876660787
PheGenIrs876660787
hapmaprs876660787
1000 genomesrs876660787
hgdprs876660787
ensemblrs876660787
gopubmedrs876660787
geneviewrs876660787
scholarrs876660787
googlers876660787
pharmgkbrs876660787
gwascentralrs876660787
openSNPrs876660787
23andMers876660787
23andMe allrs876660787
SNP Nexus

SNPshotrs876660787
SNPdbers876660787
MSV3drs876660787
GWAS Ctlgrs876660787
Max Magnitude0
ClinVar
Risk rs876660787(T;T)
Alt rs876660787(T;T)
Reference rs876660787(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.45798631T>A
CLNSRC
CLNACC RCV000216618.1,