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rs387906228

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs387906228(-;-)
Make rs387906228(-;AG)
ReferenceGRCh38 38.1/141
Chromosome5
Position112801279
GeneAPC
is asnp
is mentioned by
dbSNPrs387906228
ebirs387906228
HLIrs387906228
Exacrs387906228
Varsomers387906228
Maprs387906228
PheGenIrs387906228
hapmaprs387906228
1000 genomesrs387906228
hgdprs387906228
ensemblrs387906228
gopubmedrs387906228
geneviewrs387906228
scholarrs387906228
googlers387906228
pharmgkbrs387906228
gwascentralrs387906228
openSNPrs387906228
23andMers387906228
23andMe allrs387906228
SNP Nexus

SNPshotrs387906228
SNPdbers387906228
MSV3drs387906228
GWAS Ctlgrs387906228
Max Magnitude0
ClinVar
Risk rs387906228(;)
Alt rs387906228(;)
Reference rs387906228(AG;AG)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112136976_112136977delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000829.2,