rs914468507
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
15
Location
31002982
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3718G>C (p.Ala1240Pro)
Allele
G
Clinical Significance
Uncertain significance