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rs794729227

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729227(A;T)
Make rs794729227(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112766360
GeneAPC
is asnp
is mentioned by
dbSNPrs794729227
ebirs794729227
HLIrs794729227
Exacrs794729227
Varsomers794729227
Maprs794729227
PheGenIrs794729227
hapmaprs794729227
1000 genomesrs794729227
hgdprs794729227
ensemblrs794729227
gopubmedrs794729227
geneviewrs794729227
scholarrs794729227
googlers794729227
pharmgkbrs794729227
gwascentralrs794729227
openSNPrs794729227
23andMers794729227
23andMe allrs794729227
SNP Nexus

SNPshotrs794729227
SNPdbers794729227
MSV3drs794729227
GWAS Ctlgrs794729227
Max Magnitude0
ClinVar
Risk rs794729227(T;T)
Alt rs794729227(T;T)
Reference rs794729227(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial cancer of breast Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112102057A>T
CLNSRC
CLNACC RCV000184048.2, RCV000232299.1,