rs2067801675
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
X
Location
154370941
Variant Type
SNP
Genes
ClinVar
Name
NM_001110556.2(FLNA):c.305T>G (p.Met102Arg)
Allele
C
Clinical Significance
Uncertain significance