rs139460525
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37833744
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_138797.4(ANKRD54):c.487C>T (p.Leu163=)
Allele
A
Clinical Significance
Benign