rs913431428
- Uncertain significance
Your Genotype
Sign InDescription
Variant interpreted as Uncertain significance and reported on 02-29-2020 by Lab or GTR ID 500031. 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
C
Alternative Allele
T
Chromosome
11
Location
65552974
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.1072G>A (p.Glu358Lys)
Allele
T
Clinical Significance
Uncertain significance