rs200761894
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
T
Chromosome
12
Location
32625776
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.2169A>C (p.Gly723=)
Allele
C
Clinical Significance
Likely benign