rs746263549
- Likely benign
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
12
Location
32611139
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1605G>A (p.Glu535=)
Allele
A
Clinical Significance
Likely benign
Name
NM_001370298.3(FGD4):c.1605G>T (p.Glu535Asp)
Allele
T
Clinical Significance
Uncertain significance