rs73415876
- Pathogenic
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
22
Location
37983536
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.249C>G (p.Tyr83Ter)
Allele
C
Clinical Significance
Pathogenic
Name
NM_006941.4(SOX10):c.249C>T (p.Tyr83=)
Allele
A
Clinical Significance
Benign/Likely benign