rs778089198
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
68118578
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.3355G>A (p.Ala1119Thr)
Allele
A
Clinical Significance
Likely pathogenic