| | GET1, GET1-SH3BGR (H89R +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR (I66R +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, GET1 (V131M +2 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR (R107H +2 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, LCA5L +1 more (T532I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (G516R +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (S498G +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, GET1 +1 more (M599T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (A414T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, LCA5L +1 more (T384M +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, LCA5L +1 more (G501A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LCA5L, GET1-SH3BGR +1 more (R360S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, GET1 +1 more (G316A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LCA5L, GET1 +1 more (K271R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LCA5L, GET1-SH3BGR +1 more (H398P +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (A262V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (A262T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, LCA5L +1 more (P254R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (E332Q +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (K325M +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LCA5L, GET1 +1 more (H189Q +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (H262D +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, GET1 +1 more (A125G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, LCA5L +1 more (R211T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (H52R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (R12Q +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (E92Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | GET1, GET1-SH3BGR +1 more (F15L) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | GET1-SH3BGR, LCA5L +1 more (E13A) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |