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rs587779803

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779803(-;-)
Make rs587779803(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112841977
GeneAPC
is asnp
is mentioned by
dbSNPrs587779803
ebirs587779803
HLIrs587779803
Exacrs587779803
Varsomers587779803
Maprs587779803
PheGenIrs587779803
hapmaprs587779803
1000 genomesrs587779803
hgdprs587779803
ensemblrs587779803
gopubmedrs587779803
geneviewrs587779803
scholarrs587779803
googlers587779803
pharmgkbrs587779803
gwascentralrs587779803
openSNPrs587779803
23andMers587779803
23andMe allrs587779803
SNP Nexus

SNPshotrs587779803
SNPdbers587779803
MSV3drs587779803
GWAS Ctlgrs587779803
Max Magnitude0
ClinVar
Risk rs587779803(;)
Alt rs587779803(;)
Reference rs587779803(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112177674delC
CLNSRC
CLNACC RCV000115110.2,