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rs863225359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs863225359(-;-)
Make rs863225359(-;GT)
Make rs863225359(GT;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840327
GeneAPC
is asnp
is mentioned by
dbSNPrs863225359
dbSNP (old)rs863225359
ClinGenrs863225359
ebirs863225359
HLIrs863225359
Exacrs863225359
Gnomadrs863225359
Varsomers863225359
Maprs863225359
PheGenIrs863225359
Biobankrs863225359
1000 genomesrs863225359
hgdprs863225359
ensemblrs863225359
gopubmedrs863225359
geneviewrs863225359
scholarrs863225359
googlers863225359
pharmgkbrs863225359
gwascentralrs863225359
openSNPrs863225359
23andMers863225359
23andMe allrs863225359
SNP Nexus

SNPshotrs863225359
SNPdbers863225359
MSV3drs863225359
GWAS Ctlgrs863225359
Max Magnitude0
ClinVar
Risk rs863225359(-;-)
Alt rs863225359(-;-)
Reference Rs863225359(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112176024_112176025delGT
CLNSRC
CLNACC RCV000202051.1,