rs760089242
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
15
Location
31002331
Variant Type
SNP
Genes
ClinVar
Name
NM_001252024.2(TRPM1):c.4369A>G (p.Met1457Val)
Allele
C
Clinical Significance
Uncertain significance