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rs397509433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509433(-;-)
Make rs397509433(-;A)
ReferenceGRCh38 38.1/141
Chromosome5
Position112841536
GeneAPC
is asnp
is mentioned by
dbSNPrs397509433
ebirs397509433
HLIrs397509433
Exacrs397509433
Varsomers397509433
Maprs397509433
PheGenIrs397509433
hapmaprs397509433
1000 genomesrs397509433
hgdprs397509433
ensemblrs397509433
gopubmedrs397509433
geneviewrs397509433
scholarrs397509433
googlers397509433
pharmgkbrs397509433
gwascentralrs397509433
openSNPrs397509433
23andMers397509433
23andMe allrs397509433
SNP Nexus

SNPshotrs397509433
SNPdbers397509433
MSV3drs397509433
GWAS Ctlgrs397509433
Max Magnitude0
ClinVar
Risk rs397509433(;)
Alt rs397509433(;)
Reference rs397509433(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112177233delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000862.5,