rs757184114
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
15
Location
31002153
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4547T>C (p.Val1516Ala)
Allele
G
Clinical Significance
Uncertain significance