rs1592514932
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
12
Location
32640266
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.2455-10T>C
Allele
C
Clinical Significance
Likely benign
T
C
12
32640266
SNP
NM_001370298.3(FGD4):c.2455-10T>C
C
Likely benign