rs140395841
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219234991
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018089.3(ANKZF1):c.1370C>T (p.Thr457Ile)
Allele
T
Clinical Significance
Benign