rs576575818
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
G
Alternative Allele
A
T
Chromosome
13
Location
39655821
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020751.3(COG6):c.95G>T (p.Cys32Phe)
Allele
T
Clinical Significance
Uncertain significance