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rs371085910

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs371085910(A;G)
Make rs371085910(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position112775655
GeneAPC
is asnp
is mentioned by
dbSNPrs371085910
ebirs371085910
HLIrs371085910
Exacrs371085910
Varsomers371085910
Maprs371085910
PheGenIrs371085910
hapmaprs371085910
1000 genomesrs371085910
hgdprs371085910
ensemblrs371085910
gopubmedrs371085910
geneviewrs371085910
scholarrs371085910
googlers371085910
pharmgkbrs371085910
gwascentralrs371085910
openSNPrs371085910
23andMers371085910
23andMe allrs371085910
SNP Nexus

SNPshotrs371085910
SNPdbers371085910
MSV3drs371085910
GWAS Ctlgrs371085910
Max Magnitude0
ClinVar
Risk rs371085910(G;G)
Alt rs371085910(G;G)
Reference rs371085910(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Colorectal adenoma Familial adenomatous polyposis 1 not specified
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Colorectal adenoma Familial adenomatous polyposis 1 not specified
Reversed 0
HGVS NC_000005.9:g.112111352A>G
CLNSRC Ambry Genetics ClinVar University of Washington
CLNACC RCV000130643.5, RCV000148370.1, RCV000206082.2, RCV000211892.2,