| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC101929710, PCSK1
+1 more (T640A +1 more) | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | CAST, LOC101929710
+1 more | Single nucleotide variant (intron variant) | Body mass index quantitative trait locus 12 +1 more | |
| | CAST, LOC101929710
+1 more (E463K +1 more) | Single nucleotide variant (missense variant) | Body mass index quantitative trait locus 12 +2 more | GConflicting classifications of pathogenicity |
| | CAST, LOC101929710
+1 more (V414M +1 more) | Single nucleotide variant (missense variant) | PCSK1-related condition +2 more | |
| | LOC101929710, CAST
+1 more (A166V +1 more) | Single nucleotide variant (missense variant) | Body mass index quantitative trait locus 12 +1 more | |
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