rs386834229
- not provided
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
11
Location
65713796
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_182710.3(KAT5):c.638T>G (p.Val213Gly)
Allele
G
Clinical Significance
not provided