rs1408854259
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
12
Location
32624459
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1953+7C>T
Allele
T
Clinical Significance
Likely benign