rs2032886425
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
15
Location
31028352
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3273C>A (p.Asn1091Lys)
Allele
T
Clinical Significance
Uncertain significance