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rs730882135

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882135(-;-)
Make rs730882135(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838743
GeneAPC
is asnp
is mentioned by
dbSNPrs730882135
dbSNP (classic)rs730882135
ClinGenrs730882135
ebirs730882135
HLIrs730882135
Exacrs730882135
Gnomadrs730882135
Varsomers730882135
LitVarrs730882135
Maprs730882135
PheGenIrs730882135
Biobankrs730882135
1000 genomesrs730882135
hgdprs730882135
ensemblrs730882135
geneviewrs730882135
scholarrs730882135
googlers730882135
pharmgkbrs730882135
gwascentralrs730882135
openSNPrs730882135
23andMers730882135
SNPshotrs730882135
SNPdbers730882135
MSV3drs730882135
GWAS Ctlgrs730882135
Max Magnitude0
ClinVar
Risk rs730882135(-;-)
Alt rs730882135(-;-)
Reference Rs730882135(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174440delC
CLNSRC
CLNACC RCV000161944.2, RCV000491386.1,