rs1157809817
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
15
Location
31002300
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4400G>A (p.Gly1467Glu)
Allele
T
Clinical Significance
Uncertain significance