rs191487005
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219225104
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001077198.3(ATG9A):c.483C>T (p.His161=)
Allele
A
Clinical Significance
Benign