rs147351423
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219250700
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006000.3(TUBA4A):c.999C>T (p.Ala333=)
Allele
A
Clinical Significance
Benign
G
A
2
219250700
SNP
NM_006000.3(TUBA4A):c.999C>T (p.Ala333=)
A
Benign