rs369084166
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
15
Location
31002940
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3760G>T (p.Glu1254Ter)
Allele
A
Clinical Significance
Uncertain significance