rs764185523
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
13
Location
39660815
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.303T>C (p.Leu101=)
Allele
C
Clinical Significance
Likely benign