rs2064833443
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
20
Location
10405278
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1682A>T (p.Asp561Val)
Allele
A
Clinical Significance
Uncertain significance