rs1452352925
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
15
Location
31032934
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2707A>T (p.Met903Leu)
Allele
A
Clinical Significance
Uncertain significance