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rs587776520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTCT;TTCT) 0 common in clinvar
Make rs587776520(-;-)
Make rs587776520(-;CTTT)
Make rs587776520(CTTT;CTTT)
ReferenceGRCh38 38.1/142
Chromosome5
Position112841176
GeneAPC
is asnp
is mentioned by
dbSNPrs587776520
ebirs587776520
HLIrs587776520
Exacrs587776520
Varsomers587776520
Maprs587776520
PheGenIrs587776520
hapmaprs587776520
1000 genomesrs587776520
hgdprs587776520
ensemblrs587776520
gopubmedrs587776520
geneviewrs587776520
scholarrs587776520
googlers587776520
pharmgkbrs587776520
gwascentralrs587776520
openSNPrs587776520
23andMers587776520
23andMe allrs587776520
SNP Nexus

SNPshotrs587776520
SNPdbers587776520
MSV3drs587776520
GWAS Ctlgrs587776520
Max Magnitude0
ClinVar
Risk rs587776520(;)
Alt rs587776520(;)
Reference rs587776520(TTCT;TTCT)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112176873_112176876delCTTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000863.2,