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rs876660439

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660439(A;A)
Make rs876660439(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112815535
GeneAPC
is asnp
is mentioned by
dbSNPrs876660439
ebirs876660439
HLIrs876660439
Exacrs876660439
Varsomers876660439
Maprs876660439
PheGenIrs876660439
hapmaprs876660439
1000 genomesrs876660439
hgdprs876660439
ensemblrs876660439
gopubmedrs876660439
geneviewrs876660439
scholarrs876660439
googlers876660439
pharmgkbrs876660439
gwascentralrs876660439
openSNPrs876660439
23andMers876660439
23andMe allrs876660439
SNP Nexus

SNPshotrs876660439
SNPdbers876660439
MSV3drs876660439
GWAS Ctlgrs876660439
Max Magnitude0
ClinVar
Risk rs876660439(A;A)
Alt rs876660439(A;A)
Reference rs876660439(T;T)
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.112151232T>A
CLNSRC
CLNACC RCV000217871.1,