rs587780082
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of a MUTYH-related familial adenomatous polyposis mutation |
Make rs587780082(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 45331835 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs587780082 |
dbSNP (classic) | rs587780082 |
ClinGen | rs587780082 |
ebi | rs587780082 |
HLI | rs587780082 |
Exac | rs587780082 |
Gnomad | rs587780082 |
Varsome | rs587780082 |
LitVar | rs587780082 |
Map | rs587780082 |
PheGenI | rs587780082 |
Biobank | rs587780082 |
1000 genomes | rs587780082 |
hgdp | rs587780082 |
ensembl | rs587780082 |
geneview | rs587780082 |
scholar | rs587780082 |
rs587780082 | |
pharmgkb | rs587780082 |
gwascentral | rs587780082 |
openSNP | rs587780082 |
23andMe | rs587780082 |
SNPshot | rs587780082 |
SNPdbe | rs587780082 |
MSV3d | rs587780082 |
GWAS Ctlg | rs587780082 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs587780082(T;T) |
Alt | rs587780082(T;T) |
Reference | Rs587780082(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis |
Variation | info |
Gene | MUTYH |
CLNDBN | Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis |
Reversed | 1 |
HGVS | NC_000001.10:g.45797507G>A |
CLNSRC | |
CLNACC | RCV000115753.7, RCV000212713.2, RCV000465024.1, |