rs1856727052
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
11
Location
65554263
Variant Type
SNP
Genes
ClinVar
Name
NM_001130144.3(LTBP3):c.449G>T (p.Gly150Val)
Allele
A
Clinical Significance
Uncertain significance