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rs876658176

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658176(-;-)
Make rs876658176(-;GA)
Make rs876658176(GA;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112780827
GeneAPC
is asnp
is mentioned by
dbSNPrs876658176
ebirs876658176
HLIrs876658176
Exacrs876658176
Varsomers876658176
Maprs876658176
PheGenIrs876658176
hapmaprs876658176
1000 genomesrs876658176
hgdprs876658176
ensemblrs876658176
gopubmedrs876658176
geneviewrs876658176
scholarrs876658176
googlers876658176
pharmgkbrs876658176
gwascentralrs876658176
openSNPrs876658176
23andMers876658176
23andMe allrs876658176
SNP Nexus

SNPshotrs876658176
SNPdbers876658176
MSV3drs876658176
GWAS Ctlgrs876658176
Max Magnitude0
ClinVar
Risk rs876658176(GA;GA)
Alt rs876658176(GA;GA)
Reference rs876658176(;)
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.112116523_112116524dupGA
CLNSRC
CLNACC RCV000214782.1,