rs370737996
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
22
Location
37771660
Variant Type
SNP
Genes
ClinVar
Name
NM_001039141.3(TRIOBP):c.6860G>A (p.Arg2287His)
Allele
A
Clinical Significance
Uncertain significance