rs281865063
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
12
Location
32611270
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1736G>A (p.Arg579His)
Allele
A
Clinical Significance
Conflicting interpretations of pathogenicity