rs201678865
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
12
Location
32601370
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.1194T>C (p.Asn398=)
Allele
C
Clinical Significance
Likely benign