rs181499296
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
15
Location
31031157
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2953A>C (p.Met985Leu)
Allele
G
Clinical Significance
Conflicting interpretations of pathogenicity