rs551481786
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
12
Location
32602148
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1248-13A>G
Allele
G
Clinical Significance
Likely benign
A
G
12
32602148
SNP
NM_001370298.3(FGD4):c.1248-13A>G
G
Likely benign