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rs876658846

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658846(C;G)
Make rs876658846(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112767234
GeneAPC
is asnp
is mentioned by
dbSNPrs876658846
ebirs876658846
HLIrs876658846
Exacrs876658846
Varsomers876658846
Maprs876658846
PheGenIrs876658846
hapmaprs876658846
1000 genomesrs876658846
hgdprs876658846
ensemblrs876658846
gopubmedrs876658846
geneviewrs876658846
scholarrs876658846
googlers876658846
pharmgkbrs876658846
gwascentralrs876658846
openSNPrs876658846
23andMers876658846
23andMe allrs876658846
SNP Nexus

SNPshotrs876658846
SNPdbers876658846
MSV3drs876658846
GWAS Ctlgrs876658846
Max Magnitude0
ClinVar
Risk rs876658846(G;G)
Alt rs876658846(G;G)
Reference rs876658846(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.112102931C>G
CLNSRC
CLNACC RCV000221332.1,