rs766396216
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
15
Location
31032792
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2849G>A (p.Arg950Gln)
Allele
T
Clinical Significance
Uncertain significance