p.G195Vfs
p.G195Vfs · SaudiVarKB evidence summary derived from retained literature mentions.
1Variant mentions
1Publications
2Associated gene records
0Associated phenotype records
Associated gene records
Co-mentioned in the same publicationsAssociated phenotype records
Co-mentioned in the same publicationsNo retained phenotype associations.
Associated population records
Co-mentioned in the same publications| Population | Identifier / context | Articles | Mentions |
|---|---|---|---|
| Saudi Arabia | Cohort 22 | 1 | 1 |
Supporting publications
1 records- 2021Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses.Orphanet journal of rare diseasesPubMed ↗