rs754207459
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
20
Location
10408660
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1129A>G (p.Asn377Asp)
Allele
C
Clinical Significance
Uncertain significance