rs63749871
- Conflicting interpretations of pathogenicity
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
12
Location
32602217
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1304T>C (p.Met435Thr)
Allele
C
Clinical Significance
Conflicting interpretations of pathogenicity
Name
NM_001370298.3(FGD4):c.1304T>G (p.Met435Arg)
Allele
G
Clinical Significance
Pathogenic