| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130005991, TM7SF2 (T29A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130005991, TM7SF2 (S39W) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130005991, TM7SF2 (G40R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Variation (no sequence alteration +1 more) | not provided | |
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