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

rs863225339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs863225339(-;-)
Make rs863225339(-;GA)
Make rs863225339(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838729
GeneAPC
is asnp
is mentioned by
dbSNPrs863225339
dbSNP (old)rs863225339
ClinGenrs863225339
ebirs863225339
HLIrs863225339
Exacrs863225339
Gnomadrs863225339
Varsomers863225339
Maprs863225339
PheGenIrs863225339
Biobankrs863225339
1000 genomesrs863225339
hgdprs863225339
ensemblrs863225339
gopubmedrs863225339
geneviewrs863225339
scholarrs863225339
googlers863225339
pharmgkbrs863225339
gwascentralrs863225339
openSNPrs863225339
23andMers863225339
23andMe allrs863225339
SNP Nexus

SNPshotrs863225339
SNPdbers863225339
MSV3drs863225339
GWAS Ctlgrs863225339
Max Magnitude0
ClinVar
Risk rs863225339(-;-)
Alt rs863225339(-;-)
Reference Rs863225339(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174426_112174427delGA
CLNSRC
CLNACC RCV000202221.1,