rs17058955
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
13
Location
39012713
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_025138.5(PROSER1):c.2539T>A (p.Ser847Thr)
Allele
T
Clinical Significance
Benign