rs781295423
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
15
Location
31002363
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4337T>A (p.Phe1446Tyr)
Allele
T
Clinical Significance
Uncertain significance