rs369751598
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
12
Location
32610841
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1602+7G>A
Allele
A
Clinical Significance
Likely benign
G
A
12
32610841
SNP
NM_001370298.3(FGD4):c.1602+7G>A
A
Likely benign