rs1557179655
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
X
Location
154367927
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.537G>C (p.Lys179Asn)
Allele
G
Clinical Significance
Conflicting interpretations of pathogenicity