ClinVar Miner

List of variants in gene INF2 reported as pathogenic for not provided

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Gene type:
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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_022489.4(INF2):c.158T>C (p.Leu53Pro)
NM_022489.4(INF2):c.217G>A (p.Gly73Ser) rs1566777560
NM_022489.4(INF2):c.653G>A (p.Arg218Gln) rs267607183
NM_022489.4(INF2):c.658G>A (p.Glu220Lys) rs530391015

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