rs200144770
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
12
Location
32640446
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.2625T>C (p.Ala875=)
Allele
C
Clinical Significance
Likely benign