rs191719470
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
15
Location
31002796
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3904G>A (p.Glu1302Lys)
Allele
T
Clinical Significance
Uncertain significance