rs137854582
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;T) | 6.5 | Familial Adenomatous Polyposis |
(T;T) | 0 | common in clinvar |
Make rs137854582(A;A) |
Make rs137854582(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112837687 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs137854582 |
dbSNP (classic) | rs137854582 |
ClinGen | rs137854582 |
ebi | rs137854582 |
HLI | rs137854582 |
Exac | rs137854582 |
Gnomad | rs137854582 |
Varsome | rs137854582 |
LitVar | rs137854582 |
Map | rs137854582 |
PheGenI | rs137854582 |
Biobank | rs137854582 |
1000 genomes | rs137854582 |
hgdp | rs137854582 |
ensembl | rs137854582 |
geneview | rs137854582 |
scholar | rs137854582 |
rs137854582 | |
pharmgkb | rs137854582 |
gwascentral | rs137854582 |
openSNP | rs137854582 |
23andMe | rs137854582 |
SNPshot | rs137854582 |
SNPdbe | rs137854582 |
MSV3d | rs137854582 |
GWAS Ctlg | rs137854582 |
Max Magnitude | 6.5 |
ClinVar | |
---|---|
Risk | rs137854582(A;A) |
Alt | rs137854582(A;A) |
Reference | Rs137854582(T;T) |
Significance | Pathogenic |
Disease | Gardner syndrome |
Variation | info |
Gene | APC |
CLNDBN | Gardner syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112173384T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000875.2, |