RS13321615 FLNB

Health Risk Chr 3:58123134 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
FLNB-Related Spectrum Disorders
Connective tissue disorder
FLNB-related disorder
Inborn genetic diseases
FLNB-Related Spectrum Disorders
Connective tissue disorder
FLNB-related disorder
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.4%
1kG ALL
99.8%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in FLNB
rs80356521 rs80356519 rs80356520 rs80356506 rs80356513 rs121908894 rs121908895 rs28937587 rs80356494 rs121908896
Ask Dr. Hemsworth about this variant