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rs587779798

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779798(A;A)
Make rs587779798(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112775742
GeneAPC
is asnp
is mentioned by
dbSNPrs587779798
ebirs587779798
HLIrs587779798
Exacrs587779798
Varsomers587779798
Maprs587779798
PheGenIrs587779798
hapmaprs587779798
1000 genomesrs587779798
hgdprs587779798
ensemblrs587779798
gopubmedrs587779798
geneviewrs587779798
scholarrs587779798
googlers587779798
pharmgkbrs587779798
gwascentralrs587779798
openSNPrs587779798
23andMers587779798
23andMe allrs587779798
SNP Nexus

SNPshotrs587779798
SNPdbers587779798
MSV3drs587779798
GWAS Ctlgrs587779798
Max Magnitude0
ClinVar
Risk rs587779798(A;A)
Alt rs587779798(A;A)
Reference rs587779798(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112111439G>A
CLNSRC
CLNACC RCV000115103.4,