rs1555418784
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
15
Location
31028470
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3155G>A (p.Cys1052Tyr)
Allele
T
Clinical Significance
Likely pathogenic