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rs876660665

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660665(A;T)
Make rs876660665(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112841538
GeneAPC
is asnp
is mentioned by
dbSNPrs876660665
ebirs876660665
HLIrs876660665
Exacrs876660665
Varsomers876660665
Maprs876660665
PheGenIrs876660665
hapmaprs876660665
1000 genomesrs876660665
hgdprs876660665
ensemblrs876660665
gopubmedrs876660665
geneviewrs876660665
scholarrs876660665
googlers876660665
pharmgkbrs876660665
gwascentralrs876660665
openSNPrs876660665
23andMers876660665
23andMe allrs876660665
SNP Nexus

SNPshotrs876660665
SNPdbers876660665
MSV3drs876660665
GWAS Ctlgrs876660665
Max Magnitude0
ClinVar
Risk rs876660665(T;T)
Alt rs876660665(T;T)
Reference rs876660665(A;A)
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.112177235A>T
CLNSRC
CLNACC RCV000217699.1,