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

rs754122018

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754122018(C;T)
Make rs754122018(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112840632
GeneAPC
is asnp
is mentioned by
dbSNPrs754122018
ebirs754122018
HLIrs754122018
Exacrs754122018
Varsomers754122018
Maprs754122018
PheGenIrs754122018
hapmaprs754122018
1000 genomesrs754122018
hgdprs754122018
ensemblrs754122018
gopubmedrs754122018
geneviewrs754122018
scholarrs754122018
googlers754122018
pharmgkbrs754122018
gwascentralrs754122018
openSNPrs754122018
23andMers754122018
23andMe allrs754122018
SNP Nexus

SNPshotrs754122018
SNPdbers754122018
MSV3drs754122018
GWAS Ctlgrs754122018
Max Magnitude0
ClinVar
Risk rs754122018(G,T;G,T)
Alt rs754122018(G,T;G,T)
Reference rs754122018(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.112176329C>T
CLNSRC
CLNACC RCV000214118.1,