rs2033151333
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
15
Location
31032780
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2861G>C (p.Cys954Ser)
Allele
G
Clinical Significance
Uncertain significance