rs746686516
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3575648
Variant Type
SNP
Genes
ClinVar
Name
NM_001011.4(RPS7):c.39C>T (p.Gly13=)
Allele
T
Clinical Significance
Uncertain significance