rs13007650
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
2
Location
219231956
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.177A>C (p.Arg59Ser)
Allele
C
Clinical Significance
Benign