rs45508796
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
39655898
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.153+19G>A
Allele
A
Clinical Significance
Benign/Likely benign