rs1553343210
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
2
Location
3580836
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.539T>A (p.Leu180His)
Allele
A
Clinical Significance
Uncertain significance