rs786205113
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
15
Location
31032930
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2711C>A (p.Ser904Ter)
Allele
T
Clinical Significance
Pathogenic