rs1555939415
- Likely pathogenic
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
22
Location
37983382
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.403A>C (p.Ser135Arg)
Allele
G
Clinical Significance
Likely pathogenic
Name
NM_006941.4(SOX10):c.403A>G (p.Ser135Gly)
Allele
C
Clinical Significance
Likely pathogenic