rs281865065
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
12
Location
32633547
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.2173-2A>G
Allele
G
Clinical Significance
Conflicting interpretations of pathogenicity