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rs876658355

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658355(C;T)
Make rs876658355(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112835073
GeneAPC
is asnp
is mentioned by
dbSNPrs876658355
ebirs876658355
HLIrs876658355
Exacrs876658355
Varsomers876658355
Maprs876658355
PheGenIrs876658355
hapmaprs876658355
1000 genomesrs876658355
hgdprs876658355
ensemblrs876658355
gopubmedrs876658355
geneviewrs876658355
scholarrs876658355
googlers876658355
pharmgkbrs876658355
gwascentralrs876658355
openSNPrs876658355
23andMers876658355
23andMe allrs876658355
SNP Nexus

SNPshotrs876658355
SNPdbers876658355
MSV3drs876658355
GWAS Ctlgrs876658355
Max Magnitude0
ClinVar
Risk rs876658355(A,T;A,T)
Alt rs876658355(A,T;A,T)
Reference rs876658355(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.112170770C>A; NC_000005.9:g.112170770C>T
CLNSRC
CLNACC RCV000217597.1, RCV000222219.1,