rs1019221239
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 112835093 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs1019221239 |
dbSNP (classic) | rs1019221239 |
ClinGen | rs1019221239 |
ebi | rs1019221239 |
HLI | rs1019221239 |
Exac | rs1019221239 |
Gnomad | rs1019221239 |
Varsome | rs1019221239 |
LitVar | rs1019221239 |
Map | rs1019221239 |
PheGenI | rs1019221239 |
Biobank | rs1019221239 |
1000 genomes | rs1019221239 |
hgdp | rs1019221239 |
ensembl | rs1019221239 |
geneview | rs1019221239 |
scholar | rs1019221239 |
rs1019221239 | |
pharmgkb | rs1019221239 |
gwascentral | rs1019221239 |
openSNP | rs1019221239 |
23andMe | rs1019221239 |
SNPshot | rs1019221239 |
SNPdbe | rs1019221239 |
MSV3d | rs1019221239 |
GWAS Ctlg | rs1019221239 |
Max Magnitude | 0 |
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, |