rs768051814
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
15
Location
31002867
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3833C>T (p.Thr1278Met)
Allele
A
Clinical Significance
Uncertain significance