rs74315515
- Pathogenic
- Pathogenic/Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
22
Location
37983381
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.404G>C (p.Ser135Thr)
Allele
G
Clinical Significance
Pathogenic
Name
NM_006941.4(SOX10):c.404G>A (p.Ser135Asn)
Allele
T
Clinical Significance
Pathogenic/Likely pathogenic