rs764504417
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
15
Location
31002987
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3713G>A (p.Arg1238Gln)
Allele
T
Clinical Significance
Uncertain significance