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rs587782305

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs587782305(-;-)
Make rs587782305(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838853
GeneAPC
is asnp
is mentioned by
dbSNPrs587782305
ebirs587782305
HLIrs587782305
Exacrs587782305
Varsomers587782305
Maprs587782305
PheGenIrs587782305
hapmaprs587782305
1000 genomesrs587782305
hgdprs587782305
ensemblrs587782305
gopubmedrs587782305
geneviewrs587782305
scholarrs587782305
googlers587782305
pharmgkbrs587782305
gwascentralrs587782305
openSNPrs587782305
23andMers587782305
23andMe allrs587782305
SNP Nexus

SNPshotrs587782305
SNPdbers587782305
MSV3drs587782305
GWAS Ctlgrs587782305
Max Magnitude0
ClinVar
Risk rs587782305(;)
Alt rs587782305(;)
Reference rs587782305(CT;CT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174550_112174551delCT
CLNSRC
CLNACC RCV000131192.2,