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rs876660774

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660774(A;T)
Make rs876660774(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45331187
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876660774
ebirs876660774
HLIrs876660774
Exacrs876660774
Varsomers876660774
Maprs876660774
PheGenIrs876660774
hapmaprs876660774
1000 genomesrs876660774
hgdprs876660774
ensemblrs876660774
gopubmedrs876660774
geneviewrs876660774
scholarrs876660774
googlers876660774
pharmgkbrs876660774
gwascentralrs876660774
openSNPrs876660774
23andMers876660774
23andMe allrs876660774
SNP Nexus

SNPshotrs876660774
SNPdbers876660774
MSV3drs876660774
GWAS Ctlgrs876660774
Max Magnitude0
ClinVar
Risk rs876660774(T;T)
Alt rs876660774(T;T)
Reference rs876660774(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.45796859T>A
CLNSRC
CLNACC RCV000219128.1,