rs1949689887
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
12
Location
32619788
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1840A>C (p.Lys614Gln)
Allele
C
Clinical Significance
Uncertain significance