rs1426680504
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219233851
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.956C>T (p.Pro319Leu)
Allele
T
Clinical Significance
Uncertain significance