rs756330364
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
22
Location
37769175
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6723G>C (p.Leu2241=)
Allele
C
Clinical Significance
Uncertain significance