rs2031838852
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
15
Location
31002852
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3848A>C (p.Gln1283Pro)
Allele
G
Clinical Significance
Uncertain significance