rs757084547
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78035532
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033022.4(RPS24):c.91G>A (p.Gly31Arg)
Allele
A
Clinical Significance
Uncertain significance