rs149055210
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
39655791
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.65A>G (p.Asn22Ser)
Allele
G
Clinical Significance
Likely benign