rs200506719
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
2
Location
219232564
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.439G>A (p.Glu147Lys)
Allele
A
Clinical Significance
Benign