rs4931641
- Benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
T
Alternative Allele
A
C
G
Chromosome
12
Location
32602124
Variant Type
SNP
Genes
ClinVar
Name
NM_001370298.3(FGD4):c.1248-37T>A
Allele
A
Clinical Significance
Benign