rs2033333662
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
15
Location
31035659
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2587T>G (p.Tyr863Asp)
Allele
C
Clinical Significance
Uncertain significance