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

rs786201134

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201134(-;-)
Make rs786201134(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112841351
GeneAPC
is asnp
is mentioned by
dbSNPrs786201134
ebirs786201134
HLIrs786201134
Exacrs786201134
Varsomers786201134
Maprs786201134
PheGenIrs786201134
hapmaprs786201134
1000 genomesrs786201134
hgdprs786201134
ensemblrs786201134
gopubmedrs786201134
geneviewrs786201134
scholarrs786201134
googlers786201134
pharmgkbrs786201134
gwascentralrs786201134
openSNPrs786201134
23andMers786201134
23andMe allrs786201134
SNP Nexus

SNPshotrs786201134
SNPdbers786201134
MSV3drs786201134
GWAS Ctlgrs786201134
Max Magnitude0
ClinVar
Risk rs786201134(;)
Alt rs786201134(;)
Reference rs786201134(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112177048delT
CLNSRC
CLNACC RCV000162741.1,