rs370469506
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
15
Location
31032826
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2815C>T (p.Arg939Cys)
Allele
A
Clinical Significance
Uncertain significance