rs1665661722
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
2
Location
5693044
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.323A>C (p.Lys108Thr)
Allele
C
Clinical Significance
Likely pathogenic