ClinVar Miner

List of variants reported as uncertain significance for Parkinson disease 17 by GeneReviews

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_018206.6(VPS35):c.151G>A (p.Gly51Ser) rs193077277
NM_018206.6(VPS35):c.1520A>T (p.Tyr507Phe) rs1555465749
NM_018206.6(VPS35):c.1570C>T (p.Arg524Trp) rs184277092
NM_018206.6(VPS35):c.1679T>C (p.Ile560Thr) rs760128592
NM_018206.6(VPS35):c.171G>A (p.Met57Ile) rs183554824
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.2210C>T (p.Ala737Val) rs749516404
NM_018206.6(VPS35):c.2320C>A (p.Leu774Met) rs192419029
NM_018206.6(VPS35):c.2359G>A (p.Glu787Lys) rs777050595
NM_018206.6(VPS35):c.723T>G (p.Ile241Met) rs192783364
NM_018206.6(VPS35):c.946C>T (p.Pro316Ser) rs770029606

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