List of variants in gene PRKN studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.111G>A (p.Pro37=)	rs77795533	0.03342
NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn)	rs1801334	0.02570
NM_004562.3(PRKN):c.574A>C (p.Met192Leu)	rs9456735	0.01850
NM_004562.3(PRKN):c.101A>G (p.Gln34Arg)	rs148851677	0.00303
NM_004562.3(PRKN):c.48G>A (p.Glu16=)	rs143477190	0.00270
NM_004562.3(PRKN):c.52G>A (p.Asp18Asn)	rs146288080	0.00074
NM_004562.3(PRKN):c.727G>A (p.Asp243Asn)	rs146173584	0.00009
NM_004562.3(PRKN):c.1000C>T (p.Arg334Cys)	rs199657839	0.00004
NM_004562.3(PRKN):c.1017G>A (p.Ala339=)	rs546676036	0.00003
NM_004562.3(PRKN):c.205A>G (p.Ile69Val)	rs766391627	0.00001
NM_004562.3(PRKN):c.1138G>C (p.Val380Leu)	rs1801582
NM_004562.3(PRKN):c.245C>A (p.Ala82Glu)	rs55774500

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