rs1555939523
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
22
Location
37983658
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.127C>T (p.Arg43Ter)
Allele
A
Clinical Significance
Pathogenic
G
A
T
22
37983658
SNP
NM_006941.4(SOX10):c.127C>T (p.Arg43Ter)
A
Pathogenic