G19D (p.Gly19Asp) variant of LAMA2 (Laminin subunit alpha-2)
G19D (p.Gly19Asp) in LAMA2 (Laminin subunit alpha-2) is a missense change. The record also includes variant effect predictions and population frequency data.
G19D (p.Gly19Asp) variant details
- p.Gly19Asp
- TOPMed rs1775916031
- gnomAD rs1775916031
- Missense
- REVEL 0.02
- CADD 2.53
- PolyPhen-2 0.00
- SIFT 0.62
- Most common in the African/African-American population (allele frequency 2.4e-05)