rs765093575
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
15
Location
31032772
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2869A>G (p.Ile957Val)
Allele
C
Clinical Significance
Uncertain significance