rs1397403248
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
C
Alternative Allele
T
Chromosome
22
Location
37973731
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1165G>A (p.Gly389Ser)
Allele
T
Clinical Significance
Uncertain significance