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rs387906229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906229(-;-)
Make rs387906229(-;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112821952
GeneAPC
is asnp
is mentioned by
dbSNPrs387906229
ebirs387906229
HLIrs387906229
Exacrs387906229
Varsomers387906229
Maprs387906229
PheGenIrs387906229
hapmaprs387906229
1000 genomesrs387906229
hgdprs387906229
ensemblrs387906229
gopubmedrs387906229
geneviewrs387906229
scholarrs387906229
googlers387906229
pharmgkbrs387906229
gwascentralrs387906229
openSNPrs387906229
23andMers387906229
23andMe allrs387906229
SNP Nexus

SNPshotrs387906229
SNPdbers387906229
MSV3drs387906229
GWAS Ctlgrs387906229
Max Magnitude0
ClinVar
Risk rs387906229(;)
Alt rs387906229(;)
Reference rs387906229(T;T)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112157649delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000831.1,