rs2031815916
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
15
Location
31002474
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4226T>A (p.Ile1409Lys)
Allele
T
Clinical Significance
Uncertain significance