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

rs1060503323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503323(A;A)
Make rs1060503323(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112780782
GeneAPC
is asnp
is mentioned by
dbSNPrs1060503323
dbSNP (classic)rs1060503323
ClinGenrs1060503323
ebirs1060503323
HLIrs1060503323
Exacrs1060503323
Gnomadrs1060503323
Varsomers1060503323
LitVarrs1060503323
Maprs1060503323
PheGenIrs1060503323
Biobankrs1060503323
1000 genomesrs1060503323
hgdprs1060503323
ensemblrs1060503323
geneviewrs1060503323
scholarrs1060503323
googlers1060503323
pharmgkbrs1060503323
gwascentralrs1060503323
openSNPrs1060503323
23andMers1060503323
SNPshotrs1060503323
SNPdbers1060503323
MSV3drs1060503323
GWAS Ctlgrs1060503323
Max Magnitude0
ClinVar
Risk rs1060503323(A;A)
Alt rs1060503323(A;A)
Reference Rs1060503323(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112116479G>A
CLNSRC
CLNACC RCV000458868.1, RCV000491376.1,