rs1661370560
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
2
Location
3580159
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.406C>G (p.Pro136Ala)
Allele
G
Clinical Significance
Uncertain significance