rs74315516
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
22
Location
37973957
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.939C>G (p.Tyr313Ter)
Allele
C
Clinical Significance
Pathogenic