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rs876660765

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660765(A;A)
Make rs876660765(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112815594
GeneAPC
is asnp
is mentioned by
dbSNPrs876660765
ebirs876660765
HLIrs876660765
Exacrs876660765
Varsomers876660765
Maprs876660765
PheGenIrs876660765
hapmaprs876660765
1000 genomesrs876660765
hgdprs876660765
ensemblrs876660765
gopubmedrs876660765
geneviewrs876660765
scholarrs876660765
googlers876660765
pharmgkbrs876660765
gwascentralrs876660765
openSNPrs876660765
23andMers876660765
23andMe allrs876660765
SNP Nexus

SNPshotrs876660765
SNPdbers876660765
MSV3drs876660765
GWAS Ctlgrs876660765
Max Magnitude0
ClinVar
Risk rs876660765(A;A)
Alt rs876660765(A;A)
Reference rs876660765(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112151291G>A
CLNSRC
CLNACC RCV000217532.1,