rs199579096
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
219251616
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006000.3(TUBA4A):c.324T>C (p.Tyr108=)
Allele
G
Clinical Significance
Benign
A
G
2
219251616
SNP
NM_006000.3(TUBA4A):c.324T>C (p.Tyr108=)
G
Benign