rs2064859899
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
20
Location
10408701
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1088T>C (p.Leu363Pro)
Allele
G
Clinical Significance
Uncertain significance