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rs876660837

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660837(G;T)
Make rs876660837(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45331335
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876660837
ebirs876660837
HLIrs876660837
Exacrs876660837
Varsomers876660837
Maprs876660837
PheGenIrs876660837
hapmaprs876660837
1000 genomesrs876660837
hgdprs876660837
ensemblrs876660837
gopubmedrs876660837
geneviewrs876660837
scholarrs876660837
googlers876660837
pharmgkbrs876660837
gwascentralrs876660837
openSNPrs876660837
23andMers876660837
23andMe allrs876660837
SNP Nexus

SNPshotrs876660837
SNPdbers876660837
MSV3drs876660837
GWAS Ctlgrs876660837
Max Magnitude0
ClinVar
Risk rs876660837(T;T)
Alt rs876660837(T;T)
Reference rs876660837(G;G)
Significance Probable-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.45797007C>A
CLNSRC
CLNACC RCV000218775.1,