rs1592364946
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
12
Location
32601346
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1170C>A (p.Ile390=)
Allele
A
Clinical Significance
Likely benign