rs372924586
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219234243
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.1159G>A (p.Asp387Asn)
Allele
A
Clinical Significance
Uncertain significance