rs554416392
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
15
Location
31002075
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4625G>C (p.Arg1542Pro)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_001252024.2(TRPM1):c.4625G>A (p.Arg1542His)
Allele
T
Clinical Significance
Uncertain significance