| | FLNB, FLNB-AS1 (P2338L +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FLNB, FLNB-AS1 (S2472W +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (S2518F +3 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | FLNB, FLNB-AS1 (E2460K +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (Y2390C +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FLNB, FLNB-AS1 (R2451C +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (K2500N +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (V2356A +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (A2551S +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (V2439L +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (D2334N +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (V2406I +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FLNB, FLNB-AS1 (A2543S +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (T2547I +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (F2406I +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (S2489R +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (G2367V +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (F2347I +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (H2344D +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (G2386S +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (D2511N +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (V2343I +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (R2411* +3 more) | Single nucleotide variant (nonsense) | not provided | |
| | FLNB, FLNB-AS1 (T2416P +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (G2453D +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FLNB, FLNB-AS1 (I2428M +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (E2422G +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FLNB, FLNB-AS1 (V2397M +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (V2516M +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (G2495V +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (T2530N +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (M2417L +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FLNB, FLNB-AS1 (S2518P +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Larsen syndrome | |
| | FLNB, FLNB-AS1 (F2502Y +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (M2421L +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (V2351A +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (T2423M +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (A2357T +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FLNB, FLNB-AS1 (E2409K +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FLNB, FLNB-AS1 (T2443N +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FLNB, FLNB-AS1 (M2417T +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FLNB, FLNB-AS1 (G2433S +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (S2392L +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (N2425D +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (E2422K +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FLNB, FLNB-AS1 (P2544R +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (A2458P +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (Y2502C +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (S2345I +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (S2457P +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (E2340K +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FLNB, FLNB-AS1 (A2365T +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (S2470L +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FLNB, FLNB-AS1 (S2506F +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (A2412V +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FLNB, FLNB-AS1 (N2459S +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (P2424S +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FLNB, FLNB-AS1 (T2385N +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (L2427V +3 more) | Single nucleotide variant (missense variant) | Larsen syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | FLNB, FLNB-AS1 (G2456D +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | FLNB, FLNB-AS1 (R2387Q +3 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |