rs118203974
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
12
Location
32601410
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1234C>T (p.Arg412Ter)
Allele
T
Clinical Significance
Pathogenic