rs1400071824
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
15
Location
31002265
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4435G>C (p.Glu1479Gln)
Allele
G
Clinical Significance
Uncertain significance