rs548475910
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
T
Chromosome
13
Location
39655660
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020751.2(COG6):c.-67A>T
Allele
T
Clinical Significance
Uncertain significance