rs759982135
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
12
Location
32640437
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2616C>T (p.Ile872=)
Allele
T
Clinical Significance
Likely benign