rs951838467
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
20
Location
10405686
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1274C>T (p.Thr425Ile)
Allele
A
Clinical Significance
Uncertain significance