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rs387906231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATAG;ATAG) 0 common in clinvar
Make rs387906231(-;-)
Make rs387906231(-;ATAG)
ReferenceGRCh38 38.1/141
Chromosome5
Position112775715
GeneAPC
is asnp
is mentioned by
dbSNPrs387906231
ebirs387906231
HLIrs387906231
Exacrs387906231
Varsomers387906231
Maprs387906231
PheGenIrs387906231
hapmaprs387906231
1000 genomesrs387906231
hgdprs387906231
ensemblrs387906231
gopubmedrs387906231
geneviewrs387906231
scholarrs387906231
googlers387906231
pharmgkbrs387906231
gwascentralrs387906231
openSNPrs387906231
23andMers387906231
23andMe allrs387906231
SNP Nexus

SNPshotrs387906231
SNPdbers387906231
MSV3drs387906231
GWAS Ctlgrs387906231
Max Magnitude0
ClinVar
Risk rs387906231(;)
Alt rs387906231(;)
Reference rs387906231(ATAG;ATAG)
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.112111412_112111415delATAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000841.3, RCV000201968.1,