rs765969178
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
12
Location
32619881
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1922+11C>T
Allele
T
Clinical Significance
Likely benign
C
T
12
32619881
SNP
NM_001370298.3(FGD4):c.1922+11C>T
T
Likely benign