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rs397515735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397515735(-;-)
Make rs397515735(-;CT)
ReferenceGRCh38 38.1/141
Chromosome5
Position112815556
GeneAPC
is asnp
is mentioned by
dbSNPrs397515735
ebirs397515735
HLIrs397515735
Exacrs397515735
Varsomers397515735
Maprs397515735
PheGenIrs397515735
hapmaprs397515735
1000 genomesrs397515735
hgdprs397515735
ensemblrs397515735
gopubmedrs397515735
geneviewrs397515735
scholarrs397515735
googlers397515735
pharmgkbrs397515735
gwascentralrs397515735
openSNPrs397515735
23andMers397515735
23andMe allrs397515735
SNP Nexus

SNPshotrs397515735
SNPdbers397515735
MSV3drs397515735
GWAS Ctlgrs397515735
Max Magnitude0
ClinVar
Risk rs397515735(;)
Alt rs397515735(;)
Reference rs397515735(CT;CT)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112151253_112151254delCT
CLNSRC ClinVar
CLNACC RCV000035084.2,