rs138775799
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in clinvar | 
| Make rs138775799(A;A) | 
| Make rs138775799(A;G) | 
| Reference | GRCh38 38.1/142 | 
| Chromosome | 1 | 
| Position | 45333472 | 
| Gene | MUTYH | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs138775799 | 
| dbSNP (classic) | rs138775799 | 
| ClinGen | rs138775799 | 
| ebi | rs138775799 | 
| HLI | rs138775799 | 
| Exac | rs138775799 | 
| Gnomad | rs138775799 | 
| Varsome | rs138775799 | 
| LitVar | rs138775799 | 
| Map | rs138775799 | 
| PheGenI | rs138775799 | 
| Biobank | rs138775799 | 
| 1000 genomes | rs138775799 | 
| hgdp | rs138775799 | 
| ensembl | rs138775799 | 
| geneview | rs138775799 | 
| scholar | rs138775799 | 
| rs138775799 | |
| pharmgkb | rs138775799 | 
| gwascentral | rs138775799 | 
| openSNP | rs138775799 | 
| 23andMe | rs138775799 | 
| SNPshot | rs138775799 | 
| SNPdbe | rs138775799 | 
| MSV3d | rs138775799 | 
| GWAS Ctlg | rs138775799 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs138775799(A;A) | 
| Alt | rs138775799(A;A) | 
| Reference | Rs138775799(G;G) | 
| 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 | 0 | 
| HGVS | NC_000001.10:g.45799144G>A | 
| CLNSRC | Ambry Genetics ClinVar | 
| CLNACC | RCV000129018.3, RCV000235267.1, RCV000471769.1, | 
