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rs387906238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs387906238(-;-)
Make rs387906238(-;AA)
ReferenceGRCh38 38.1/141
Chromosome5
Position112819224
GeneAPC
is asnp
is mentioned by
dbSNPrs387906238
ebirs387906238
HLIrs387906238
Exacrs387906238
Varsomers387906238
Maprs387906238
PheGenIrs387906238
hapmaprs387906238
1000 genomesrs387906238
hgdprs387906238
ensemblrs387906238
gopubmedrs387906238
geneviewrs387906238
scholarrs387906238
googlers387906238
pharmgkbrs387906238
gwascentralrs387906238
openSNPrs387906238
23andMers387906238
23andMe allrs387906238
SNP Nexus

SNPshotrs387906238
SNPdbers387906238
MSV3drs387906238
GWAS Ctlgrs387906238
Max Magnitude0
ClinVar
Risk rs387906238(;)
Alt rs387906238(;)
Reference rs387906238(AA;AA)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 not provided
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 not provided
Reversed 0
HGVS NC_000005.9:g.112154921_112154922delAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000871.2, RCV000159588.2,



[PMID 26681312OA-icon.png] Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.