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rs387906235

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAG;AGAG) 0 common in clinvar
Make rs387906235(-;-)
Make rs387906235(-;AGAG)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839985
GeneAPC
is asnp
is mentioned by
dbSNPrs387906235
dbSNP (classic)rs387906235
ClinGenrs387906235
ebirs387906235
HLIrs387906235
Exacrs387906235
Gnomadrs387906235
Varsomers387906235
LitVarrs387906235
Maprs387906235
PheGenIrs387906235
Biobankrs387906235
1000 genomesrs387906235
hgdprs387906235
ensemblrs387906235
geneviewrs387906235
scholarrs387906235
googlers387906235
pharmgkbrs387906235
gwascentralrs387906235
openSNPrs387906235
23andMers387906235
SNPshotrs387906235
SNPdbers387906235
MSV3drs387906235
GWAS Ctlgrs387906235
Max Magnitude0
ClinVar
Risk rs387906235(-;-)
Alt rs387906235(-;-)
Reference Rs387906235(AGAG;AGAG)
Significance Pathogenic
Disease Periampullary adenoma Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Periampullary adenoma Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175682_112175685delAGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000851.4, RCV000474620.1,