rs1950619446
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
12
Location
32633625
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2249A>C (p.Asp750Ala)
Allele
C
Clinical Significance
Uncertain significance