rs752584934
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
15
Location
31031021
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3089G>C (p.Trp1030Ser)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_001252024.2(TRPM1):c.3089G>T (p.Trp1030Leu)
Allele
A
Clinical Significance
Uncertain significance