rs533778281
- Uncertain significance
Your Genotype
Sign InDescription
Regulation of SOX10 expression
Reference Allele
G
Alternative Allele
C
Chromosome
22
Location
38016774
Variant Type
SNP
Genes
LOC101927099
ClinVar
Name
NM_001301130.2(POLR2F):c.453-24294G>C
Allele
C
Clinical Significance
Uncertain significance