rs201837886
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
15
Location
31002777
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3923A>T (p.Asp1308Val)
Allele
A
Clinical Significance
Uncertain significance