rs751838063
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
2
Location
5693573
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.852G>C (p.Ser284=)
Allele
C
Clinical Significance
Likely benign