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rs876659652

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659652(-;-)
Make rs876659652(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112840752
GeneAPC
is asnp
is mentioned by
dbSNPrs876659652
ebirs876659652
HLIrs876659652
Exacrs876659652
Varsomers876659652
Maprs876659652
PheGenIrs876659652
hapmaprs876659652
1000 genomesrs876659652
hgdprs876659652
ensemblrs876659652
gopubmedrs876659652
geneviewrs876659652
scholarrs876659652
googlers876659652
pharmgkbrs876659652
gwascentralrs876659652
openSNPrs876659652
23andMers876659652
23andMe allrs876659652
SNP Nexus

SNPshotrs876659652
SNPdbers876659652
MSV3drs876659652
GWAS Ctlgrs876659652
Max Magnitude0
ClinVar
Risk rs876659652(;)
Alt rs876659652(;)
Reference rs876659652(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.112176449delG
CLNSRC
CLNACC RCV000219835.1,