rs748046539
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
15
Location
31028451
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3174T>A (p.Asp1058Glu)
Allele
T
Clinical Significance
Likely pathogenic