rs545371712
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
13
Location
39655860
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.134C>T (p.Thr45Met)
Allele
T
Clinical Significance
Uncertain significance