rs144301422
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
15
Location
31031122
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2988G>A (p.Leu996=)
Allele
T
Clinical Significance
Benign