rs532487848
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
20
Location
10405306
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1654G>A (p.Ala552Thr)
Allele
T
Clinical Significance
Uncertain significance