rs1857215256
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
11
Location
65716922
Variant Type
SNP
Genes
ClinVar
Name
NM_182710.3(KAT5):c.1204T>A (p.Cys402Ser)
Allele
A
Clinical Significance
Pathogenic
T
A
11
65716922
SNP
NM_182710.3(KAT5):c.1204T>A (p.Cys402Ser)
A
Pathogenic