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

rs786202351

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202351(G;G)
Make rs786202351(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112780905
GeneAPC
is asnp
is mentioned by
dbSNPrs786202351
ebirs786202351
HLIrs786202351
Exacrs786202351
Varsomers786202351
Maprs786202351
PheGenIrs786202351
hapmaprs786202351
1000 genomesrs786202351
hgdprs786202351
ensemblrs786202351
gopubmedrs786202351
geneviewrs786202351
scholarrs786202351
googlers786202351
pharmgkbrs786202351
gwascentralrs786202351
openSNPrs786202351
23andMers786202351
23andMe allrs786202351
SNP Nexus

SNPshotrs786202351
SNPdbers786202351
MSV3drs786202351
GWAS Ctlgrs786202351
Max Magnitude0
ClinVar
Risk rs786202351(G;G)
Alt rs786202351(G;G)
Reference rs786202351(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112116602T>G
CLNSRC
CLNACC RCV000165115.1,