rs1427885318
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
15
Location
31031144
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2966T>C (p.Leu989Pro)
Allele
G
Clinical Significance
Uncertain significance