rs1555901905
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
22
Location
37772621
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6957A>G (p.Gly2319=)
Allele
G
Clinical Significance
Uncertain significance