rs779085438
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
15
Location
31003061
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3639T>C (p.Asn1213=)
Allele
G
Clinical Significance
Likely benign