ClinVar Miner

List of variants in gene CHCHD2 studied for Parkinson disease 22, autosomal dominant

Included ClinVar conditions (1):
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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_016139.4(CHCHD2):c.101C>T (p.Pro34Leu) rs371198317 0.00014
NM_016139.4(CHCHD2):c.300+5G>A rs750014782 0.00002
NM_016139.4(CHCHD2):c.182C>T (p.Thr61Ile) rs864309650
NM_016139.4(CHCHD2):c.434G>A (p.Arg145Gln) rs752169833

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