rs137854569
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 6.5 | Familial Adenomatous Polyposis |
Make rs137854569(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112815499 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs137854569 |
dbSNP (classic) | rs137854569 |
ClinGen | rs137854569 |
ebi | rs137854569 |
HLI | rs137854569 |
Exac | rs137854569 |
Gnomad | rs137854569 |
Varsome | rs137854569 |
LitVar | rs137854569 |
Map | rs137854569 |
PheGenI | rs137854569 |
Biobank | rs137854569 |
1000 genomes | rs137854569 |
hgdp | rs137854569 |
ensembl | rs137854569 |
geneview | rs137854569 |
scholar | rs137854569 |
rs137854569 | |
pharmgkb | rs137854569 |
gwascentral | rs137854569 |
openSNP | rs137854569 |
23andMe | rs137854569 |
SNPshot | rs137854569 |
SNPdbe | rs137854569 |
MSV3d | rs137854569 |
GWAS Ctlg | rs137854569 |
Max Magnitude | 6.5 |
ClinVar | |
---|---|
Risk | rs137854569(G;G) rs137854569(T;T) |
Alt | rs137854569(G;G) rs137854569(T;T) |
Reference | Rs137854569(C;C) |
Significance | Pathogenic |
Disease | Gardner syndrome Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | APC |
CLNDBN | Gardner syndrome Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112151196C>G; NC_000005.9:g.112151196C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000836.5, RCV000218327.1, |