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rs879253785

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253785(A;A)
Make rs879253785(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112707528
GeneAPC
is asnp
is mentioned by
dbSNPrs879253785
ebirs879253785
HLIrs879253785
Exacrs879253785
Varsomers879253785
Maprs879253785
PheGenIrs879253785
hapmaprs879253785
1000 genomesrs879253785
hgdprs879253785
ensemblrs879253785
gopubmedrs879253785
geneviewrs879253785
scholarrs879253785
googlers879253785
pharmgkbrs879253785
gwascentralrs879253785
openSNPrs879253785
23andMers879253785
23andMe allrs879253785
SNP Nexus

SNPshotrs879253785
SNPdbers879253785
MSV3drs879253785
GWAS Ctlgrs879253785
Max Magnitude0
ClinVar
Risk rs879253785(A;A)
Alt rs879253785(A;A)
Reference rs879253785(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112043225G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234994.1,