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rs876659015

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659015(-;-)
Make rs876659015(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112841567
GeneAPC
is asnp
is mentioned by
dbSNPrs876659015
ebirs876659015
HLIrs876659015
Exacrs876659015
Varsomers876659015
Maprs876659015
PheGenIrs876659015
hapmaprs876659015
1000 genomesrs876659015
hgdprs876659015
ensemblrs876659015
gopubmedrs876659015
geneviewrs876659015
scholarrs876659015
googlers876659015
pharmgkbrs876659015
gwascentralrs876659015
openSNPrs876659015
23andMers876659015
23andMe allrs876659015
SNP Nexus

SNPshotrs876659015
SNPdbers876659015
MSV3drs876659015
GWAS Ctlgrs876659015
Max Magnitude0
ClinVar
Risk rs876659015(;)
Alt rs876659015(;)
Reference rs876659015(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.112177264delG
CLNSRC
CLNACC RCV000220550.1,