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rs863225331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225331(-;-)
Make rs863225331(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838353
GeneAPC
is asnp
is mentioned by
dbSNPrs863225331
dbSNP (classic)rs863225331
ClinGenrs863225331
ebirs863225331
HLIrs863225331
Exacrs863225331
Gnomadrs863225331
Varsomers863225331
LitVarrs863225331
Maprs863225331
PheGenIrs863225331
Biobankrs863225331
1000 genomesrs863225331
hgdprs863225331
ensemblrs863225331
geneviewrs863225331
scholarrs863225331
googlers863225331
pharmgkbrs863225331
gwascentralrs863225331
openSNPrs863225331
23andMers863225331
SNPshotrs863225331
SNPdbers863225331
MSV3drs863225331
GWAS Ctlgrs863225331
Max Magnitude0
ClinVar
Risk rs863225331(-;-)
Alt rs863225331(-;-)
Reference Rs863225331(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174050delA
CLNSRC
CLNACC RCV000202122.1,