rs782615607
- Benign/Likely benign
Your Genotype
Sign InDescription
Rare (0.1%) in general population databases (dbsnp, esp, 1000 genomes) ;Rarity in general population databases (dbsnp, esp, 1000 genomes);Synonymous alterations with insufficient evidence to classify as benign
Synonymous alterations with insufficient evidence to classify as benign;Rarity in general population databases (dbsnp, esp, 1000 genomes);Rare (0.1%) in general population databases (dbsnp, esp, 1000 genomes)
Reference Allele
C
Alternative Allele
T
Chromosome
X
Location
154365240
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.1587G>A (p.Lys529=)
Allele
T
Clinical Significance
Benign/Likely benign