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

rs878853419

From SNPedia

Orientationplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs878853419(AT;AT)
Make rs878853419(AT;CC)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112835073
GeneAPC
is asnp
is mentioned by
dbSNPrs878853419
ebirs878853419
HLIrs878853419
Exacrs878853419
Varsomers878853419
Maprs878853419
PheGenIrs878853419
hapmaprs878853419
1000 genomesrs878853419
hgdprs878853419
ensemblrs878853419
gopubmedrs878853419
geneviewrs878853419
scholarrs878853419
googlers878853419
pharmgkbrs878853419
gwascentralrs878853419
openSNPrs878853419
23andMers878853419
23andMe allrs878853419
SNP Nexus

SNPshotrs878853419
SNPdbers878853419
MSV3drs878853419
GWAS Ctlgrs878853419
Max Magnitude0
ClinVar
Risk rs878853419(AT;AT)
Alt rs878853419(AT;AT)
Reference rs878853419(CC;CC)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112170770_112170771delCCinsAT
CLNSRC
CLNACC RCV000229977.1,