rs755934741
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
12
Location
32608054
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1502G>C (p.Arg501Thr)
Allele
C
Clinical Significance
Uncertain significance