rs144178741
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
3576496
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.157G>A (p.Val53Ile)
Allele
A
Clinical Significance
Uncertain significance