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rs876659676

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659676(A;G)
Make rs876659676(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332252
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876659676
ebirs876659676
HLIrs876659676
Exacrs876659676
Varsomers876659676
Maprs876659676
PheGenIrs876659676
hapmaprs876659676
1000 genomesrs876659676
hgdprs876659676
ensemblrs876659676
gopubmedrs876659676
geneviewrs876659676
scholarrs876659676
googlers876659676
pharmgkbrs876659676
gwascentralrs876659676
openSNPrs876659676
23andMers876659676
23andMe allrs876659676
SNP Nexus

SNPshotrs876659676
SNPdbers876659676
MSV3drs876659676
GWAS Ctlgrs876659676
Max Magnitude0
ClinVar
Risk rs876659676(G;G)
Alt rs876659676(G;G)
Reference rs876659676(A;A)
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.45797924T>C
CLNSRC
CLNACC RCV000216419.1,