rs758351673
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
15
Location
31032699
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.2942T>C (p.Ile981Thr)
Allele
G
Clinical Significance
Uncertain significance