rs147538692
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
68077436
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.1609G>A (p.Val537Ile)
Allele
A
Clinical Significance
Likely benign