| | LOC130063123, S1PR4 (A17V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063123, S1PR4 (G19S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063123, S1PR4 (R23Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063123, S1PR4 (Y29C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063123, S1PR4 (G37R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063123, S1PR4 (R50Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (V162I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (G177R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (R203C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (R203H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (G214S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (R239H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (A241V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (R248H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (C324R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130063124, S1PR4 (D352N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |