rs373443346
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
15
Location
31002249
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4451C>T (p.Thr1484Met)
Allele
A
Clinical Significance
Uncertain significance