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rs730881272

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881272(-;-)
Make rs730881272(-;GA)
Make rs730881272(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839067
GeneAPC
is asnp
is mentioned by
dbSNPrs730881272
ebirs730881272
HLIrs730881272
Exacrs730881272
Varsomers730881272
Maprs730881272
PheGenIrs730881272
hapmaprs730881272
1000 genomesrs730881272
hgdprs730881272
ensemblrs730881272
gopubmedrs730881272
geneviewrs730881272
scholarrs730881272
googlers730881272
pharmgkbrs730881272
gwascentralrs730881272
openSNPrs730881272
23andMers730881272
23andMe allrs730881272
SNP Nexus

SNPshotrs730881272
SNPdbers730881272
MSV3drs730881272
GWAS Ctlgrs730881272
Max Magnitude0
ClinVar
Risk rs730881272(GA;GA)
Alt rs730881272(GA;GA)
Reference rs730881272(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174764_112174765insGA
CLNSRC
CLNACC RCV000159589.1,