rs730880026
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219250740
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006000.3(TUBA4A):c.959G>A (p.Arg320His)
Allele
T
Clinical Significance
Pathogenic