rs200339260
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
2
Location
219235545
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.1763T>C (p.Met588Thr)
Allele
C
Clinical Significance
Uncertain significance