rs587777480
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
2
Location
5692899
Variant Type
SNP
ClinVar
Name
NM_003108.4(SOX11):c.178T>C (p.Ser60Pro)
Allele
C
Clinical Significance
Pathogenic
T
C
2
5692899
SNP
NM_003108.4(SOX11):c.178T>C (p.Ser60Pro)
C
Pathogenic