rs2031796075
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
15
Location
31002191
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4509T>C (p.His1503=)
Allele
G
Clinical Significance
Uncertain significance