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rs876659517

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659517(C;T)
Make rs876659517(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112835080
GeneAPC
is asnp
is mentioned by
dbSNPrs876659517
ebirs876659517
HLIrs876659517
Exacrs876659517
Varsomers876659517
Maprs876659517
PheGenIrs876659517
hapmaprs876659517
1000 genomesrs876659517
hgdprs876659517
ensemblrs876659517
gopubmedrs876659517
geneviewrs876659517
scholarrs876659517
googlers876659517
pharmgkbrs876659517
gwascentralrs876659517
openSNPrs876659517
23andMers876659517
23andMe allrs876659517
SNP Nexus

SNPshotrs876659517
SNPdbers876659517
MSV3drs876659517
GWAS Ctlgrs876659517
Max Magnitude0
ClinVar
Risk rs876659517(T;T)
Alt rs876659517(T;T)
Reference rs876659517(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.112170777C>T
CLNSRC
CLNACC RCV000215115.1,