rs1224103433
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
12
Location
32602197
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1284A>G (p.Lys428=)
Allele
G
Clinical Significance
Likely benign