rs745401697
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
5692883
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_003108.4(SOX11):c.162C>T (p.Asn54=)
Allele
T
Clinical Significance
Likely benign