rs757962189
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
15
Location
31002930
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3770C>A (p.Ala1257Glu)
Allele
T
Clinical Significance
Uncertain significance