| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RAB37, CD300LF (G275S +2 more) | Single nucleotide variant (3 prime UTR variant +3 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (L276P +2 more) | Single nucleotide variant (3 prime UTR variant +3 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (Y249C +2 more) | Single nucleotide variant (3 prime UTR variant +3 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (T225M +2 more) | Single nucleotide variant (synonymous variant +3 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (D202N +6 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (K154Q +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (T93M +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (R79P +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (I58L +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (R55Q +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (S47L +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CD300LF, RAB37 (T37I +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene