rs782198156
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
X
Location
154368041
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.423C>T (p.Ile141=)
Allele
A
Clinical Significance
Benign
G
A
X
154368041
SNP
NM_001110556.2(FLNA):c.423C>T (p.Ile141=)
A
Benign