ClinVar Miner

List of variants in gene ALOXE3, LOC126862485 studied for hereditary skin disorder

Included ClinVar conditions (790):
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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_001165960.1(ALOXE3):c.32C>T (p.Pro11Leu) rs3027232 0.27769
NM_021628.3(ALOXE3):c.-300C>G rs3027229 0.14510
NM_021628.3(ALOXE3):c.-99C>G rs112227180 0.02269
NM_021628.3(ALOXE3):c.-304G>T rs79377087 0.00560
NM_021628.3(ALOXE3):c.-295T>C rs575913104 0.00034
NM_021628.3(ALOXE3):c.-247G>A rs1052642860 0.00001
NM_021628.3(ALOXE3):c.-260G>A rs886053584 0.00001
NM_021628.3(ALOXE3):c.-266C>A rs886053585 0.00001
NM_021628.3(ALOXE3):c.-337G>T rs886053586 0.00001
NM_021628.3(ALOXE3):c.-178GA[3]
NM_021628.3(ALOXE3):c.34C>T (p.Pro12Ser) rs893544249
NM_021628.3(ALOXE3):c.38_41del (p.Pro12_Tyr13insTer) rs769980324
NM_021628.3(ALOXE3):c.57_63del (p.Asp20fs) rs1980748884
NM_021628.3(ALOXE3):c.75_76insGAC (p.Thr25_Leu26insAsp) rs2151848449

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