List of variants studied for Parkinson disease 17 by GeneReviews

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Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_018206.6(VPS35):c.151G>A (p.Gly51Ser)	rs193077277	0.00028
NM_018206.6(VPS35):c.946C>T (p.Pro316Ser)	rs770029606	0.00009
NM_018206.6(VPS35):c.2320C>A (p.Leu774Met)	rs192419029	0.00006
NM_018206.6(VPS35):c.2210C>T (p.Ala737Val)	rs749516404	0.00002
NM_018206.6(VPS35):c.1520A>T (p.Tyr507Phe)	rs1555465749	0.00001
NM_018206.6(VPS35):c.1570C>T (p.Arg524Trp)	rs184277092	0.00001
NM_018206.6(VPS35):c.1679T>C (p.Ile560Thr)	rs760128592	0.00001
NM_018206.6(VPS35):c.171G>A (p.Met57Ile)	rs183554824	0.00001
NM_018206.6(VPS35):c.1796A>G (p.His599Arg)	rs1434487321
NM_018206.6(VPS35):c.1819A>G (p.Met607Val)	rs1555523076
NM_018206.6(VPS35):c.1858G>A (p.Asp620Asn)	rs188286943
NM_018206.6(VPS35):c.2359G>A (p.Glu787Lys)	rs777050595
NM_018206.6(VPS35):c.723T>G (p.Ile241Met)	rs192783364

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