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rs587779794

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779794(-;-)
Make rs587779794(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112840469
GeneAPC
is asnp
is mentioned by
dbSNPrs587779794
ebirs587779794
HLIrs587779794
Exacrs587779794
Varsomers587779794
Maprs587779794
PheGenIrs587779794
hapmaprs587779794
1000 genomesrs587779794
hgdprs587779794
ensemblrs587779794
gopubmedrs587779794
geneviewrs587779794
scholarrs587779794
googlers587779794
pharmgkbrs587779794
gwascentralrs587779794
openSNPrs587779794
23andMers587779794
23andMe allrs587779794
SNP Nexus

SNPshotrs587779794
SNPdbers587779794
MSV3drs587779794
GWAS Ctlgrs587779794
Max Magnitude0
ClinVar
Risk rs587779794(;)
Alt rs587779794(;)
Reference rs587779794(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112176166delA
CLNSRC
CLNACC RCV000115097.3,