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rs876658538

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658538(-;-)
Make rs876658538(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112819156
GeneAPC
is asnp
is mentioned by
dbSNPrs876658538
ebirs876658538
HLIrs876658538
Exacrs876658538
Varsomers876658538
Maprs876658538
PheGenIrs876658538
hapmaprs876658538
1000 genomesrs876658538
hgdprs876658538
ensemblrs876658538
gopubmedrs876658538
geneviewrs876658538
scholarrs876658538
googlers876658538
pharmgkbrs876658538
gwascentralrs876658538
openSNPrs876658538
23andMers876658538
23andMe allrs876658538
SNP Nexus

SNPshotrs876658538
SNPdbers876658538
MSV3drs876658538
GWAS Ctlgrs876658538
Max Magnitude0
ClinVar
Risk rs876658538(;)
Alt rs876658538(;)
Reference rs876658538(G;G)
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.112154853delG
CLNSRC
CLNACC RCV000221309.1,