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rs863225327

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225327(A;A)
Make rs863225327(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112767188
GeneAPC
is asnp
is mentioned by
dbSNPrs863225327
ebirs863225327
HLIrs863225327
Exacrs863225327
Varsomers863225327
Maprs863225327
PheGenIrs863225327
hapmaprs863225327
1000 genomesrs863225327
hgdprs863225327
ensemblrs863225327
gopubmedrs863225327
geneviewrs863225327
scholarrs863225327
googlers863225327
pharmgkbrs863225327
gwascentralrs863225327
openSNPrs863225327
23andMers863225327
23andMe allrs863225327
SNP Nexus

SNPshotrs863225327
SNPdbers863225327
MSV3drs863225327
GWAS Ctlgrs863225327
Max Magnitude0
ClinVar
Risk rs863225327(A,C;A,C)
Alt rs863225327(A,C;A,C)
Reference rs863225327(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.112102885G>A; NC_000005.9:g.112102885G>C
CLNSRC
CLNACC RCV000201979.1, RCV000213314.1,