rs1807584458
- not provided
Your Genotype
Sign InDescription
Variant interpretted as Uncertain significance and reported on 02-24-2017 by Lab or GTR ID 26957. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.
Reference Allele
T
Alternative Allele
A
Chromosome
8
Location
68022056
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.357T>A (p.Tyr119Ter)
Allele
A
Clinical Significance
not provided