rs745675837
- 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
A
T
Chromosome
2
Location
5693508
Variant Type
SNP
Genes
ClinVar
Name
NM_003108.4(SOX11):c.787C>A (p.Pro263Thr)
Allele
A
Clinical Significance
Uncertain significance