rs1949117700
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
12
Location
32611269
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1735C>T (p.Arg579Cys)
Allele
T
Clinical Significance
Uncertain significance