rs773514635
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
12
Location
32611201
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1667C>T (p.Pro556Leu)
Allele
T
Clinical Significance
Uncertain significance