rs200400906
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3580186
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.433C>T (p.Arg145Cys)
Allele
T
Clinical Significance
Uncertain significance