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rs387906233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906233(-;-)
Make rs387906233(-;A)
Make rs387906233(A;A)
ReferenceGRCh38 38.1/141
Chromosome5
Position112835092
GeneAPC
is asnp
is mentioned by
dbSNPrs387906233
ebirs387906233
HLIrs387906233
Exacrs387906233
Varsomers387906233
Maprs387906233
PheGenIrs387906233
hapmaprs387906233
1000 genomesrs387906233
hgdprs387906233
ensemblrs387906233
gopubmedrs387906233
geneviewrs387906233
scholarrs387906233
googlers387906233
pharmgkbrs387906233
gwascentralrs387906233
openSNPrs387906233
23andMers387906233
23andMe allrs387906233
SNP Nexus

SNPshotrs387906233
SNPdbers387906233
MSV3drs387906233
GWAS Ctlgrs387906233
Max Magnitude0
ClinVar
Risk rs387906233(A;A)
Alt rs387906233(A;A)
Reference rs387906233(;)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112170789_112170790insA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000847.2,