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rs876660454

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876660454(-;-)
Make rs876660454(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112840300
GeneAPC
is asnp
is mentioned by
dbSNPrs876660454
ebirs876660454
HLIrs876660454
Exacrs876660454
Varsomers876660454
Maprs876660454
PheGenIrs876660454
hapmaprs876660454
1000 genomesrs876660454
hgdprs876660454
ensemblrs876660454
gopubmedrs876660454
geneviewrs876660454
scholarrs876660454
googlers876660454
pharmgkbrs876660454
gwascentralrs876660454
openSNPrs876660454
23andMers876660454
23andMe allrs876660454
SNP Nexus

SNPshotrs876660454
SNPdbers876660454
MSV3drs876660454
GWAS Ctlgrs876660454
Max Magnitude0
ClinVar
Risk rs876660454(;)
Alt rs876660454(;)
Reference rs876660454(AT;AT)
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.112175997_112175998delAT
CLNSRC
CLNACC RCV000220260.1,