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rs876658868

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658868(C;T)
Make rs876658868(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112827116
GeneAPC
is asnp
is mentioned by
dbSNPrs876658868
ebirs876658868
HLIrs876658868
Exacrs876658868
Varsomers876658868
Maprs876658868
PheGenIrs876658868
hapmaprs876658868
1000 genomesrs876658868
hgdprs876658868
ensemblrs876658868
gopubmedrs876658868
geneviewrs876658868
scholarrs876658868
googlers876658868
pharmgkbrs876658868
gwascentralrs876658868
openSNPrs876658868
23andMers876658868
23andMe allrs876658868
SNP Nexus

SNPshotrs876658868
SNPdbers876658868
MSV3drs876658868
GWAS Ctlgrs876658868
Max Magnitude0
ClinVar
Risk rs876658868(T;T)
Alt rs876658868(T;T)
Reference rs876658868(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.112162813C>T
CLNSRC
CLNACC RCV000219498.1,