rs4645914
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65712785
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_182710.3(KAT5):c.198C>T (p.Ser66=)
Allele
T
Clinical Significance
Benign
C
T
11
65712785
SNP
NM_182710.3(KAT5):c.198C>T (p.Ser66=)
T
Benign