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rs387906232

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906232(-;-)
Make rs387906232(-;A)
Make rs387906232(A;A)
ReferenceGRCh38 38.1/141
Chromosome5
Position112819101
GeneAPC
is asnp
is mentioned by
dbSNPrs387906232
ebirs387906232
HLIrs387906232
Exacrs387906232
Varsomers387906232
Maprs387906232
PheGenIrs387906232
hapmaprs387906232
1000 genomesrs387906232
hgdprs387906232
ensemblrs387906232
gopubmedrs387906232
geneviewrs387906232
scholarrs387906232
googlers387906232
pharmgkbrs387906232
gwascentralrs387906232
openSNPrs387906232
23andMers387906232
23andMe allrs387906232
SNP Nexus

SNPshotrs387906232
SNPdbers387906232
MSV3drs387906232
GWAS Ctlgrs387906232
Max Magnitude0
ClinVar
Risk rs387906232(A;A)
Alt rs387906232(A;A)
Reference rs387906232(;)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112154798dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000842.2,