Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881273

From SNPedia

Orientationplus
Geno Mag Summary
(AATG;AATG) 0 common in clinvar
Make rs730881273(-;-)
Make rs730881273(-;TGAA)
Make rs730881273(TGAA;TGAA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112841084
GeneAPC
is asnp
is mentioned by
dbSNPrs730881273
ebirs730881273
HLIrs730881273
Exacrs730881273
Varsomers730881273
Maprs730881273
PheGenIrs730881273
hapmaprs730881273
1000 genomesrs730881273
hgdprs730881273
ensemblrs730881273
gopubmedrs730881273
geneviewrs730881273
scholarrs730881273
googlers730881273
pharmgkbrs730881273
gwascentralrs730881273
openSNPrs730881273
23andMers730881273
23andMe allrs730881273
SNP Nexus

SNPshotrs730881273
SNPdbers730881273
MSV3drs730881273
GWAS Ctlgrs730881273
Max Magnitude0
ClinVar
Risk rs730881273(;)
Alt rs730881273(;)
Reference rs730881273(AATG;AATG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112176781_112176784delTGAA
CLNSRC
CLNACC RCV000159590.1, RCV000234000.1,