rs757337069
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
39655849
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.123G>A (p.Lys41=)
Allele
A
Clinical Significance
Likely benign