rs193920825
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
68069831
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.1444-4G>A
Allele
A
Clinical Significance
Uncertain significance