rs151182040
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
2
Location
219224027
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001077198.3(ATG9A):c.1266-5A>G
Allele
C
Clinical Significance
Benign
T
A
C
2
219224027
SNP
NM_001077198.3(ATG9A):c.1266-5A>G
C
Benign