rs146261996
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
13
Location
39659471
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020751.3(COG6):c.261T>C (p.Asn87=)
Allele
C
Clinical Significance
Likely benign