rs370076000
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
15
Location
31002700
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4000G>A (p.Val1334Met)
Allele
T
Clinical Significance
Uncertain significance