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rs138367627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs138367627(G;G)
Make rs138367627(G;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position112840326
GeneAPC
is asnp
is mentioned by
dbSNPrs138367627
ebirs138367627
HLIrs138367627
Exacrs138367627
Varsomers138367627
Maprs138367627
PheGenIrs138367627
hapmaprs138367627
1000 genomesrs138367627
hgdprs138367627
ensemblrs138367627
gopubmedrs138367627
geneviewrs138367627
scholarrs138367627
googlers138367627
pharmgkbrs138367627
gwascentralrs138367627
openSNPrs138367627
23andMers138367627
23andMe allrs138367627
SNP Nexus

SNPshotrs138367627
SNPdbers138367627
MSV3drs138367627
GWAS Ctlgrs138367627
Max Magnitude0
ClinVar
Risk rs138367627(G;G)
Alt rs138367627(G;G)
Reference rs138367627(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Colorectal adenoma Familial adenomatous polyposis 1 not provided
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Colorectal adenoma Familial adenomatous polyposis 1 not provided
Reversed 0
HGVS NC_000005.9:g.112176023T>G
CLNSRC Ambry Genetics ClinVar University of Washington
CLNACC RCV000129037.2, RCV000148367.1, RCV000206222.2, RCV000236515.1,