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rs863224817

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224817(-;T)
Make rs863224817(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112835093
GeneAPC
is asnp
is mentioned by
dbSNPrs863224817
dbSNP (old)rs863224817
ClinGenrs863224817
ebirs863224817
HLIrs863224817
Exacrs863224817
Gnomadrs863224817
Varsomers863224817
Maprs863224817
PheGenIrs863224817
Biobankrs863224817
1000 genomesrs863224817
hgdprs863224817
ensemblrs863224817
gopubmedrs863224817
geneviewrs863224817
scholarrs863224817
googlers863224817
pharmgkbrs863224817
gwascentralrs863224817
openSNPrs863224817
23andMers863224817
23andMe allrs863224817
SNP Nexus

SNPshotrs863224817
SNPdbers863224817
MSV3drs863224817
GWAS Ctlgrs863224817
Max Magnitude0
ClinVar
Risk rs863224817(T;T)
Alt rs863224817(T;T)
Reference Rs863224817(-;-)
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.112170790dupT
CLNSRC
CLNACC RCV000195881.1, RCV000493455.1,