rs200797987
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
15
Location
31002109
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.4591C>A (p.His1531Asn)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_001252024.2(TRPM1):c.4591C>T (p.His1531Tyr)
Allele
A
Clinical Significance
Uncertain significance