rs879680059
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
15
Location
31003017
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3683T>G (p.Met1228Arg)
Allele
C
Clinical Significance
Uncertain significance