G19V (p.Gly19Val) variant of LAMA2 (Laminin subunit alpha-2)
G19V (p.Gly19Val) in LAMA2 (Laminin subunit alpha-2) is a missense change. The record also includes variant effect predictions and population frequency data.
G19V (p.Gly19Val) variant details
- p.Gly19Val
- TOPMed rs1775916031
- gnomAD rs1775916031
- Missense
- REVEL 0.02
- CADD 6.37
- PolyPhen-2 0.04
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)