rs1949089197
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
12
Location
32610794
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1562C>T (p.Ser521Phe)
Allele
T
Clinical Significance
Uncertain significance