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rs876658941

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658941(G;T)
Make rs876658941(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112766410
GeneAPC
is asnp
is mentioned by
dbSNPrs876658941
ebirs876658941
HLIrs876658941
Exacrs876658941
Varsomers876658941
Maprs876658941
PheGenIrs876658941
hapmaprs876658941
1000 genomesrs876658941
hgdprs876658941
ensemblrs876658941
gopubmedrs876658941
geneviewrs876658941
scholarrs876658941
googlers876658941
pharmgkbrs876658941
gwascentralrs876658941
openSNPrs876658941
23andMers876658941
23andMe allrs876658941
SNP Nexus

SNPshotrs876658941
SNPdbers876658941
MSV3drs876658941
GWAS Ctlgrs876658941
Max Magnitude0
ClinVar
Risk rs876658941(T;T)
Alt rs876658941(T;T)
Reference rs876658941(G;G)
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.112102107G>T
CLNSRC
CLNACC RCV000215333.1,