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rs876658472

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658472(-;-)
Make rs876658472(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838164
GeneAPC
is asnp
is mentioned by
dbSNPrs876658472
ebirs876658472
HLIrs876658472
Exacrs876658472
Varsomers876658472
Maprs876658472
PheGenIrs876658472
hapmaprs876658472
1000 genomesrs876658472
hgdprs876658472
ensemblrs876658472
gopubmedrs876658472
geneviewrs876658472
scholarrs876658472
googlers876658472
pharmgkbrs876658472
gwascentralrs876658472
openSNPrs876658472
23andMers876658472
23andMe allrs876658472
SNP Nexus

SNPshotrs876658472
SNPdbers876658472
MSV3drs876658472
GWAS Ctlgrs876658472
Max Magnitude0
ClinVar
Risk rs876658472(;)
Alt rs876658472(;)
Reference rs876658472(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.112173861delG
CLNSRC
CLNACC RCV000216864.1,