rs754122018
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs754122018(C;T) |
Make rs754122018(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 112840632 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs754122018 |
dbSNP (classic) | rs754122018 |
ClinGen | rs754122018 |
ebi | rs754122018 |
HLI | rs754122018 |
Exac | rs754122018 |
Gnomad | rs754122018 |
Varsome | rs754122018 |
LitVar | rs754122018 |
Map | rs754122018 |
PheGenI | rs754122018 |
Biobank | rs754122018 |
1000 genomes | rs754122018 |
hgdp | rs754122018 |
ensembl | rs754122018 |
geneview | rs754122018 |
scholar | rs754122018 |
rs754122018 | |
pharmgkb | rs754122018 |
gwascentral | rs754122018 |
openSNP | rs754122018 |
23andMe | rs754122018 |
SNPshot | rs754122018 |
SNPdbe | rs754122018 |
MSV3d | rs754122018 |
GWAS Ctlg | rs754122018 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754122018(G;G) rs754122018(T;T) |
Alt | rs754122018(G;G) rs754122018(T;T) |
Reference | Rs754122018(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | APC |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112176329C>T |
CLNSRC | |
CLNACC | RCV000214118.1, |