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rs863224456

From SNPedia

Merged intors587779352
Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAAC;AAAAC) 0 common in clinvar
Make rs863224456(-;-)
Make rs863224456(-;AAAAC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838774
GeneAPC
is asnp
is mentioned by
dbSNPrs863224456
dbSNP (old)rs863224456
ClinGenrs863224456
ebirs863224456
HLIrs863224456
Exacrs863224456
Varsomers863224456
Maprs863224456
PheGenIrs863224456
Biobankrs863224456
1000 genomesrs863224456
hgdprs863224456
ensemblrs863224456
gopubmedrs863224456
geneviewrs863224456
scholarrs863224456
googlers863224456
pharmgkbrs863224456
gwascentralrs863224456
openSNPrs863224456
23andMers863224456
23andMe allrs863224456
SNP Nexus

SNPshotrs863224456
SNPdbers863224456
MSV3drs863224456
GWAS Ctlgrs863224456
StatusMerged into rs587779352
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863224456(AAAAC;AAAAC)
Significance Pathogenic
Disease not provided Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN not provided Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174474_112174478delACAAA
CLNSRC HGMD
CLNACC RCV000077987.5, RCV000144562.4, RCV000162768.2,