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rs587781451

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781451(-;-)
Make rs587781451(-;T)
Make rs587781451(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112818967
GeneAPC
is asnp
is mentioned by
dbSNPrs587781451
ebirs587781451
HLIrs587781451
Exacrs587781451
Varsomers587781451
Maprs587781451
PheGenIrs587781451
hapmaprs587781451
1000 genomesrs587781451
hgdprs587781451
ensemblrs587781451
gopubmedrs587781451
geneviewrs587781451
scholarrs587781451
googlers587781451
pharmgkbrs587781451
gwascentralrs587781451
openSNPrs587781451
23andMers587781451
23andMe allrs587781451
SNP Nexus

SNPshotrs587781451
SNPdbers587781451
MSV3drs587781451
GWAS Ctlgrs587781451
Max Magnitude0
ClinVar
Risk rs587781451(T;T)
Alt rs587781451(T;T)
Reference rs587781451(;)
Significance Other
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000005.9:g.112154664dupT
CLNSRC
CLNACC RCV000129375.2, RCV000202006.2,