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rs730881228

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs730881228(-;-)
Make rs730881228(-;AT)
Make rs730881228(AT;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112819347
GeneAPC
is asnp
is mentioned by
dbSNPrs730881228
ebirs730881228
HLIrs730881228
Exacrs730881228
Varsomers730881228
Maprs730881228
PheGenIrs730881228
hapmaprs730881228
1000 genomesrs730881228
hgdprs730881228
ensemblrs730881228
gopubmedrs730881228
geneviewrs730881228
scholarrs730881228
googlers730881228
pharmgkbrs730881228
gwascentralrs730881228
openSNPrs730881228
23andMers730881228
23andMe allrs730881228
SNP Nexus

SNPshotrs730881228
SNPdbers730881228
MSV3drs730881228
GWAS Ctlgrs730881228
Max Magnitude0
ClinVar
Risk rs730881228(;)
Alt rs730881228(;)
Reference rs730881228(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112155044_112155045delAT
CLNSRC
CLNACC RCV000159517.1, RCV000198238.1,