rs751459846
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
15
Location
31002358
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4342G>A (p.Asp1448Asn)
Allele
T
Clinical Significance
Uncertain significance