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rs876659022

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659022(G;G)
Make rs876659022(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112841938
GeneAPC
is asnp
is mentioned by
dbSNPrs876659022
ebirs876659022
HLIrs876659022
Exacrs876659022
Varsomers876659022
Maprs876659022
PheGenIrs876659022
hapmaprs876659022
1000 genomesrs876659022
hgdprs876659022
ensemblrs876659022
gopubmedrs876659022
geneviewrs876659022
scholarrs876659022
googlers876659022
pharmgkbrs876659022
gwascentralrs876659022
openSNPrs876659022
23andMers876659022
23andMe allrs876659022
SNP Nexus

SNPshotrs876659022
SNPdbers876659022
MSV3drs876659022
GWAS Ctlgrs876659022
Max Magnitude0
ClinVar
Risk rs876659022(G;G)
Alt rs876659022(G;G)
Reference rs876659022(T;T)
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.112177635T>G
CLNSRC
CLNACC RCV000217426.1,