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rs876660816

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660816(-;-)
Make rs876660816(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112841875
GeneAPC
is asnp
is mentioned by
dbSNPrs876660816
ebirs876660816
HLIrs876660816
Exacrs876660816
Varsomers876660816
Maprs876660816
PheGenIrs876660816
hapmaprs876660816
1000 genomesrs876660816
hgdprs876660816
ensemblrs876660816
gopubmedrs876660816
geneviewrs876660816
scholarrs876660816
googlers876660816
pharmgkbrs876660816
gwascentralrs876660816
openSNPrs876660816
23andMers876660816
23andMe allrs876660816
SNP Nexus

SNPshotrs876660816
SNPdbers876660816
MSV3drs876660816
GWAS Ctlgrs876660816
Max Magnitude0
ClinVar
Risk rs876660816(;)
Alt rs876660816(;)
Reference rs876660816(C;C)
Significance Probable-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.112177572delC
CLNSRC
CLNACC RCV000221437.1,