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rs876660802

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660802(C;T)
Make rs876660802(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112819266
GeneAPC
is asnp
is mentioned by
dbSNPrs876660802
ebirs876660802
HLIrs876660802
Exacrs876660802
Varsomers876660802
Maprs876660802
PheGenIrs876660802
hapmaprs876660802
1000 genomesrs876660802
hgdprs876660802
ensemblrs876660802
gopubmedrs876660802
geneviewrs876660802
scholarrs876660802
googlers876660802
pharmgkbrs876660802
gwascentralrs876660802
openSNPrs876660802
23andMers876660802
23andMe allrs876660802
SNP Nexus

SNPshotrs876660802
SNPdbers876660802
MSV3drs876660802
GWAS Ctlgrs876660802
Max Magnitude0
ClinVar
Risk rs876660802(T;T)
Alt rs876660802(T;T)
Reference rs876660802(C;C)
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.112154963C>T
CLNSRC
CLNACC RCV000214229.1,