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rs775126020

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775126020(C;G)
Make rs775126020(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112819026
GeneAPC
is asnp
is mentioned by
dbSNPrs775126020
ebirs775126020
HLIrs775126020
Exacrs775126020
Varsomers775126020
Maprs775126020
PheGenIrs775126020
hapmaprs775126020
1000 genomesrs775126020
hgdprs775126020
ensemblrs775126020
gopubmedrs775126020
geneviewrs775126020
scholarrs775126020
googlers775126020
pharmgkbrs775126020
gwascentralrs775126020
openSNPrs775126020
23andMers775126020
23andMe allrs775126020
SNP Nexus

SNPshotrs775126020
SNPdbers775126020
MSV3drs775126020
GWAS Ctlgrs775126020
Max Magnitude0
ClinVar
Risk rs775126020(G,T;G,T)
Alt rs775126020(G,T;G,T)
Reference rs775126020(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000005.9:g.112154723C>T
CLNSRC
CLNACC RCV000164280.1, RCV000202243.2,