Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659973

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659973(C;C)
Make rs876659973(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112775738
GeneAPC
is asnp
is mentioned by
dbSNPrs876659973
ebirs876659973
HLIrs876659973
Exacrs876659973
Varsomers876659973
Maprs876659973
PheGenIrs876659973
hapmaprs876659973
1000 genomesrs876659973
hgdprs876659973
ensemblrs876659973
gopubmedrs876659973
geneviewrs876659973
scholarrs876659973
googlers876659973
pharmgkbrs876659973
gwascentralrs876659973
openSNPrs876659973
23andMers876659973
23andMe allrs876659973
SNP Nexus

SNPshotrs876659973
SNPdbers876659973
MSV3drs876659973
GWAS Ctlgrs876659973
Max Magnitude0
ClinVar
Risk rs876659973(C;C)
Alt rs876659973(C;C)
Reference rs876659973(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.112111435G>C
CLNSRC
CLNACC RCV000217536.1,