rs774889847
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
15
Location
31026161
Variant Type
SNP
Genes
LOC105370752
Phenotypes
ClinVar
Name
NM_001252024.2(TRPM1):c.3607C>A (p.Arg1203Ser)
Allele
T
Clinical Significance
Uncertain significance