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rs1019221239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112835093
GeneAPC
is asnp
is mentioned by
dbSNPrs1019221239
dbSNP (classic)rs1019221239
ClinGenrs1019221239
ebirs1019221239
HLIrs1019221239
Exacrs1019221239
Gnomadrs1019221239
Varsomers1019221239
LitVarrs1019221239
Maprs1019221239
PheGenIrs1019221239
Biobankrs1019221239
1000 genomesrs1019221239
hgdprs1019221239
ensemblrs1019221239
geneviewrs1019221239
scholarrs1019221239
googlers1019221239
pharmgkbrs1019221239
gwascentralrs1019221239
openSNPrs1019221239
23andMers1019221239
23andMe allrs1019221239
SNPshotrs1019221239
SNPdbers1019221239
MSV3drs1019221239
GWAS Ctlgrs1019221239
Max Magnitude0
ClinVar
Risk rs1019221239(C;C)
Alt rs1019221239(C;C)
Reference Rs1019221239(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112170790T>G
CLNSRC
CLNACC RCV000493755.1,