rs876660837
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 3 | Carrier of a MUTYH-related familial adenomatous polyposis mutation |
Make rs876660837(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 45331335 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs876660837 |
dbSNP (classic) | rs876660837 |
ClinGen | rs876660837 |
ebi | rs876660837 |
HLI | rs876660837 |
Exac | rs876660837 |
Gnomad | rs876660837 |
Varsome | rs876660837 |
LitVar | rs876660837 |
Map | rs876660837 |
PheGenI | rs876660837 |
Biobank | rs876660837 |
1000 genomes | rs876660837 |
hgdp | rs876660837 |
ensembl | rs876660837 |
geneview | rs876660837 |
scholar | rs876660837 |
rs876660837 | |
pharmgkb | rs876660837 |
gwascentral | rs876660837 |
openSNP | rs876660837 |
23andMe | rs876660837 |
SNPshot | rs876660837 |
SNPdbe | rs876660837 |
MSV3d | rs876660837 |
GWAS Ctlg | rs876660837 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs876660837(T;T) |
Alt | rs876660837(T;T) |
Reference | Rs876660837(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MUTYH |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000001.10:g.45797007C>A |
CLNSRC | |
CLNACC | RCV000218775.1, |