ClinVar Miner

List of variants in gene AMMECR1 reported as pathogenic for Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

Included ClinVar conditions (1):
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Gene type:
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Total variants: 3
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HGVS dbSNP
NM_015365.3(AMMECR1):c.429T>A (p.Tyr143Ter) rs765498367
NM_015365.3(AMMECR1):c.502C>T (p.Arg168Ter) rs1057519338
NM_015365.3(AMMECR1):c.530G>A (p.Gly177Asp) rs1057519337

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