rs200626788
- Conflicting interpretations of pathogenicity
- Likely benign
Your Genotype
Sign InDescription
Synonymous alterations with insufficient evidence to classify as benign
Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Reference Allele
C
Alternative Allele
A
G
Chromosome
X
Location
154371009
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.237G>C (p.Ala79=)
Allele
G
Clinical Significance
Conflicting interpretations of pathogenicity
Name
NM_001110556.2(FLNA):c.237G>T (p.Ala79=)
Allele
A
Clinical Significance
Likely benign