ClinVar Miner

List of variants in gene ANKRD11 reported as likely pathogenic by Institute for Human Genetics, University Hospital Essen

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.1711_1723del (p.Thr571fs) rs2151763044
NM_013275.6(ANKRD11):c.7411_7422del (p.Thr2471_Gly2474del) rs2151729118
NM_013275.6(ANKRD11):c.7470+2T>C rs2151728875

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