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rs876658667

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658667(A;A)
Make rs876658667(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838740
GeneAPC
is asnp
is mentioned by
dbSNPrs876658667
ebirs876658667
HLIrs876658667
Exacrs876658667
Varsomers876658667
Maprs876658667
PheGenIrs876658667
hapmaprs876658667
1000 genomesrs876658667
hgdprs876658667
ensemblrs876658667
gopubmedrs876658667
geneviewrs876658667
scholarrs876658667
googlers876658667
pharmgkbrs876658667
gwascentralrs876658667
openSNPrs876658667
23andMers876658667
23andMe allrs876658667
SNP Nexus

SNPshotrs876658667
SNPdbers876658667
MSV3drs876658667
GWAS Ctlgrs876658667
Max Magnitude0
ClinVar
Risk rs876658667(A;A)
Alt rs876658667(A;A)
Reference rs876658667(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.112174437G>A
CLNSRC
CLNACC RCV000216288.1,