rs748071139
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
20
Location
10407629
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1259A>G (p.Tyr420Cys)
Allele
C
Clinical Significance
Uncertain significance