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rs876659460

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659460(G;G)
Make rs876659460(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112835109
GeneAPC
is asnp
is mentioned by
dbSNPrs876659460
ebirs876659460
HLIrs876659460
Exacrs876659460
Varsomers876659460
Maprs876659460
PheGenIrs876659460
hapmaprs876659460
1000 genomesrs876659460
hgdprs876659460
ensemblrs876659460
gopubmedrs876659460
geneviewrs876659460
scholarrs876659460
googlers876659460
pharmgkbrs876659460
gwascentralrs876659460
openSNPrs876659460
23andMers876659460
23andMe allrs876659460
SNP Nexus

SNPshotrs876659460
SNPdbers876659460
MSV3drs876659460
GWAS Ctlgrs876659460
Max Magnitude0
ClinVar
Risk rs876659460(G;G)
Alt rs876659460(G;G)
Reference rs876659460(T;T)
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.112170806T>G
CLNSRC
CLNACC RCV000222920.1,