rs1220106574
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
12
Location
32619757
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1809A>T (p.Thr603=)
Allele
T
Clinical Significance
Likely benign