rs397515370
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
22
Location
37974200
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.698-2A>C
Allele
G
Clinical Significance
Pathogenic
T
G
22
37974200
SNP
NM_006941.4(SOX10):c.698-2A>C
G
Pathogenic