rs2031808060
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
15
Location
31002354
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4346A>G (p.Glu1449Gly)
Allele
C
Clinical Significance
Uncertain significance