rs397515457
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
22
Location
37983783
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.2T>G (p.Met1Arg)
Allele
C
Clinical Significance
Pathogenic
A
C
22
37983783
SNP
NM_006941.4(SOX10):c.2T>G (p.Met1Arg)
C
Pathogenic