rs367980245
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
20
Location
10407721
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1167G>A (p.Thr389=)
Allele
T
Clinical Significance
Likely benign