rs745728640
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
20
Location
10408722
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1067G>T (p.Gly356Val)
Allele
A
Clinical Significance
Uncertain significance