rs1932460904
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37983356
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.428+1G>A
Allele
T
Clinical Significance
Pathogenic
C
T
22
37983356
SNP
NM_006941.4(SOX10):c.428+1G>A
T
Pathogenic