rs2032741633
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
15
Location
31026228
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3540C>G (p.Phe1180Leu)
Allele
C
Clinical Significance
Uncertain significance