rs267607140
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
15
Location
31028454
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3171T>A (p.Tyr1057Ter)
Allele
T
Clinical Significance
Pathogenic