rs143057951
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37977964
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.600C>T (p.Thr200=)
Allele
A
Clinical Significance
Benign
G
A
22
37977964
SNP
NM_006941.4(SOX10):c.600C>T (p.Thr200=)
A
Benign