| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062625, RELCH (P145L) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130062624, RELCH (S11N) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130062624, RELCH (S11R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130062625, RELCH (A90T) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130062625, RELCH (T88N) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130062625, RELCH (G83R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | LOC130062625, RELCH (S76L) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC132090500, RELCH (P352S) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
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