rs915603269
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
15
Location
31026175
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3593C>A (p.Ser1198Ter)
Allele
T
Clinical Significance
Likely pathogenic