rs606231342
- Likely pathogenic
Your Genotype
Sign InDescription
Regulation of SOX10 expression
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
38016208
Variant Type
SNP
Genes
LOC101927099
ClinVar
Name
NM_001301130.2(POLR2F):c.453-24860G>A
Allele
A
Clinical Significance
Likely pathogenic