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rs587783035

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783035(A;G)
Make rs587783035(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112834949
GeneAPC
is asnp
is mentioned by
dbSNPrs587783035
ebirs587783035
HLIrs587783035
Exacrs587783035
Varsomers587783035
Maprs587783035
PheGenIrs587783035
hapmaprs587783035
1000 genomesrs587783035
hgdprs587783035
ensemblrs587783035
gopubmedrs587783035
geneviewrs587783035
scholarrs587783035
googlers587783035
pharmgkbrs587783035
gwascentralrs587783035
openSNPrs587783035
23andMers587783035
23andMe allrs587783035
SNP Nexus

SNPshotrs587783035
SNPdbers587783035
MSV3drs587783035
GWAS Ctlgrs587783035
Max Magnitude0
ClinVar
Risk rs587783035(G;G)
Alt rs587783035(G;G)
Reference rs587783035(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112170646A>G
CLNSRC
CLNACC RCV000144573.1,