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rs876659280

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659280(C;G)
Make rs876659280(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112843309
GeneAPC
is asnp
is mentioned by
dbSNPrs876659280
ebirs876659280
HLIrs876659280
Exacrs876659280
Varsomers876659280
Maprs876659280
PheGenIrs876659280
hapmaprs876659280
1000 genomesrs876659280
hgdprs876659280
ensemblrs876659280
gopubmedrs876659280
geneviewrs876659280
scholarrs876659280
googlers876659280
pharmgkbrs876659280
gwascentralrs876659280
openSNPrs876659280
23andMers876659280
23andMe allrs876659280
SNP Nexus

SNPshotrs876659280
SNPdbers876659280
MSV3drs876659280
GWAS Ctlgrs876659280
Max Magnitude0
ClinVar
Risk rs876659280(G;G)
Alt rs876659280(G;G)
Reference rs876659280(C;C)
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.112179006C>G
CLNSRC
CLNACC RCV000222855.1,