rs776107451
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
20
Location
10405449
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.1511G>A (p.Ser504Asn)
Allele
T
Clinical Significance
Uncertain significance