rs61737832
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
22
Location
37875900
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_016091.4(EIF3L):c.966A>G (p.Ala322=)
Allele
G
Clinical Significance
Benign
A
G
22
37875900
SNP
NM_016091.4(EIF3L):c.966A>G (p.Ala322=)
G
Benign