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rs876659539

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659539(C;T)
Make rs876659539(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838805
GeneAPC
is asnp
is mentioned by
dbSNPrs876659539
ebirs876659539
HLIrs876659539
Exacrs876659539
Varsomers876659539
Maprs876659539
PheGenIrs876659539
hapmaprs876659539
1000 genomesrs876659539
hgdprs876659539
ensemblrs876659539
gopubmedrs876659539
geneviewrs876659539
scholarrs876659539
googlers876659539
pharmgkbrs876659539
gwascentralrs876659539
openSNPrs876659539
23andMers876659539
23andMe allrs876659539
SNP Nexus

SNPshotrs876659539
SNPdbers876659539
MSV3drs876659539
GWAS Ctlgrs876659539
Max Magnitude0
ClinVar
Risk rs876659539(T;T)
Alt rs876659539(T;T)
Reference rs876659539(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.112174502C>T
CLNSRC
CLNACC RCV000214546.1,