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rs786204118

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204118(G;T)
Make rs786204118(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112815585
GeneAPC
is asnp
is mentioned by
dbSNPrs786204118
ebirs786204118
HLIrs786204118
Exacrs786204118
Varsomers786204118
Maprs786204118
PheGenIrs786204118
hapmaprs786204118
1000 genomesrs786204118
hgdprs786204118
ensemblrs786204118
gopubmedrs786204118
geneviewrs786204118
scholarrs786204118
googlers786204118
pharmgkbrs786204118
gwascentralrs786204118
openSNPrs786204118
23andMers786204118
23andMe allrs786204118
SNP Nexus

SNPshotrs786204118
SNPdbers786204118
MSV3drs786204118
GWAS Ctlgrs786204118
Max Magnitude0
ClinVar
Risk rs786204118(T;T)
Alt rs786204118(T;T)
Reference rs786204118(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112151282G>T
CLNSRC
CLNACC RCV000168066.1,