Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225340

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225340(A;A)
Make rs863225340(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838741
GeneAPC
is asnp
is mentioned by
dbSNPrs863225340
ebirs863225340
HLIrs863225340
Exacrs863225340
Varsomers863225340
Maprs863225340
PheGenIrs863225340
hapmaprs863225340
1000 genomesrs863225340
hgdprs863225340
ensemblrs863225340
gopubmedrs863225340
geneviewrs863225340
scholarrs863225340
googlers863225340
pharmgkbrs863225340
gwascentralrs863225340
openSNPrs863225340
23andMers863225340
23andMe allrs863225340
SNP Nexus

SNPshotrs863225340
SNPdbers863225340
MSV3drs863225340
GWAS Ctlgrs863225340
Max Magnitude0
ClinVar
Risk rs863225340(A;A)
Alt rs863225340(A;A)
Reference rs863225340(G;G)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112174438G>A
CLNSRC
CLNACC RCV000202067.1, RCV000218609.1,