rs148246113
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
13
Location
39655845
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.119A>G (p.His40Arg)
Allele
G
Clinical Significance
Uncertain significance