rs747993448
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs747993448(A;A) |
Make rs747993448(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 45332795 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs747993448 |
dbSNP (classic) | rs747993448 |
ClinGen | rs747993448 |
ebi | rs747993448 |
HLI | rs747993448 |
Exac | rs747993448 |
Gnomad | rs747993448 |
Varsome | rs747993448 |
LitVar | rs747993448 |
Map | rs747993448 |
PheGenI | rs747993448 |
Biobank | rs747993448 |
1000 genomes | rs747993448 |
hgdp | rs747993448 |
ensembl | rs747993448 |
geneview | rs747993448 |
scholar | rs747993448 |
rs747993448 | |
pharmgkb | rs747993448 |
gwascentral | rs747993448 |
openSNP | rs747993448 |
23andMe | rs747993448 |
SNPshot | rs747993448 |
SNPdbe | rs747993448 |
MSV3d | rs747993448 |
GWAS Ctlg | rs747993448 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747993448(A;A) |
Alt | rs747993448(A;A) |
Reference | Rs747993448(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided |
Variation | info |
Gene | MUTYH |
CLNDBN | Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.45798467G>A |
CLNSRC | |
CLNACC | RCV000166998.2, RCV000229525.2, RCV000236750.1, |