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rs876658811

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658811(G;T)
Make rs876658811(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112827230
GeneAPC
is asnp
is mentioned by
dbSNPrs876658811
ebirs876658811
HLIrs876658811
Exacrs876658811
Varsomers876658811
Maprs876658811
PheGenIrs876658811
hapmaprs876658811
1000 genomesrs876658811
hgdprs876658811
ensemblrs876658811
gopubmedrs876658811
geneviewrs876658811
scholarrs876658811
googlers876658811
pharmgkbrs876658811
gwascentralrs876658811
openSNPrs876658811
23andMers876658811
23andMe allrs876658811
SNP Nexus

SNPshotrs876658811
SNPdbers876658811
MSV3drs876658811
GWAS Ctlgrs876658811
Max Magnitude0
ClinVar
Risk rs876658811(T;T)
Alt rs876658811(T;T)
Reference rs876658811(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.112162927G>T
CLNSRC
CLNACC RCV000220669.1,