rs202181932
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
9
Location
113056670
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003408.3(ZFP37):c.19G>C (p.Val7Leu)
Allele
G
Clinical Significance
Uncertain significance