rs766173103
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
15
Location
31037767
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2515G>A (p.Gly839Arg)
Allele
T
Clinical Significance
Uncertain significance