rs1267263830
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
15
Location
31026262
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3506T>G (p.Leu1169Arg)
Allele
C
Clinical Significance
Uncertain significance