rs1555224749
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
12
Location
32638681
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2340C>A (p.Asn780Lys)
Allele
A
Clinical Significance
Uncertain significance