rs907657345
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
12
Location
32633665
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.2289A>C (p.Glu763Asp)
Allele
C
Clinical Significance
Uncertain significance