rs1665662335
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
5693080
Variant Type
SNP
ClinVar
Name
NM_003108.4(SOX11):c.359C>T (p.Pro120Leu)
Allele
T
Clinical Significance
Likely pathogenic