rs572580501
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
15
Location
31032739
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2902T>C (p.Phe968Leu)
Allele
G
Clinical Significance
Uncertain significance