rs1572360947
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
2
Location
3580816
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.519T>A (p.Phe173Leu)
Allele
A
Clinical Significance
Uncertain significance