ClinVar Miner

List of variants in gene combination ALOX12B, LOC130060196 reported by Institute for Human Genetics, University Medical Center Freiburg

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_001139.3(ALOX12B):c.769C>G (p.His257Asp) rs1233776328
NM_001139.3(ALOX12B):c.771_772del (p.His257fs) rs1977172596
NM_001139.3(ALOX12B):c.786CTT[1] (p.Phe264del) rs1302782570
NM_001139.3(ALOX12B):c.793G>A (p.Gly265Arg) rs1977171852
NM_001139.3(ALOX12B):c.814G>T (p.Val272Phe) rs1308351316

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