Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs387906237(-;-)
Make rs387906237(-;CT)
ReferenceGRCh38 38.1/141
Chromosome5
Position112819130
GeneAPC
is asnp
is mentioned by
dbSNPrs387906237
ebirs387906237
HLIrs387906237
Exacrs387906237
Varsomers387906237
Maprs387906237
PheGenIrs387906237
hapmaprs387906237
1000 genomesrs387906237
hgdprs387906237
ensemblrs387906237
gopubmedrs387906237
geneviewrs387906237
scholarrs387906237
googlers387906237
pharmgkbrs387906237
gwascentralrs387906237
openSNPrs387906237
23andMers387906237
23andMe allrs387906237
SNP Nexus

SNPshotrs387906237
SNPdbers387906237
MSV3drs387906237
GWAS Ctlgrs387906237
Max Magnitude0
ClinVar
Risk rs387906237(;)
Alt rs387906237(;)
Reference rs387906237(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.112154827_112154828delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000870.2,