rs730880029
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
2
Location
219251266
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006000.3(TUBA4A):c.433A>C (p.Thr145Pro)
Allele
G
Clinical Significance
Pathogenic