rs768687662
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
15
Location
31028334
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3291C>T (p.Phe1097=)
Allele
A
Clinical Significance
Likely benign