List of variants in gene CHCHD2 reported as pathogenic for Parkinson disease 22, autosomal dominant

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
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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