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rs876658724

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658724(-;-)
Make rs876658724(-;A)
Make rs876658724(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838661
GeneAPC
is asnp
is mentioned by
dbSNPrs876658724
ebirs876658724
HLIrs876658724
Exacrs876658724
Varsomers876658724
Maprs876658724
PheGenIrs876658724
hapmaprs876658724
1000 genomesrs876658724
hgdprs876658724
ensemblrs876658724
gopubmedrs876658724
geneviewrs876658724
scholarrs876658724
googlers876658724
pharmgkbrs876658724
gwascentralrs876658724
openSNPrs876658724
23andMers876658724
23andMe allrs876658724
SNP Nexus

SNPshotrs876658724
SNPdbers876658724
MSV3drs876658724
GWAS Ctlgrs876658724
Max Magnitude0
ClinVar
Risk rs876658724(A;A)
Alt rs876658724(A;A)
Reference rs876658724(;)
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.112174358dupA
CLNSRC
CLNACC RCV000214795.1,