ClinVar Miner

List of variants reported as uncertain significance for Parkinson disease 17 by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_018206.6(VPS35):c.*161C>T
NM_018206.6(VPS35):c.*276A>C rs886052009
NM_018206.6(VPS35):c.*283C>A
NM_018206.6(VPS35):c.*345T>G
NM_018206.6(VPS35):c.*380G>A rs886052004
NM_018206.6(VPS35):c.*401G>A rs553790361
NM_018206.6(VPS35):c.*575A>T
NM_018206.6(VPS35):c.*617A>G rs746602580
NM_018206.6(VPS35):c.-19C>T rs573920049
NM_018206.6(VPS35):c.-35C>G
NM_018206.6(VPS35):c.1035G>A (p.Glu345=) rs563975281
NM_018206.6(VPS35):c.1488T>C (p.His496=) rs776877370
NM_018206.6(VPS35):c.1525-5G>T
NM_018206.6(VPS35):c.1809A>T (p.Ala603=)
NM_018206.6(VPS35):c.1900A>G (p.Thr634Ala)
NM_018206.6(VPS35):c.1912A>T (p.Met638Leu) rs144997996
NM_018206.6(VPS35):c.2073C>T (p.His691=)
NM_018206.6(VPS35):c.2211+11T>C
NM_018206.6(VPS35):c.2353G>C (p.Glu785Gln)
NM_018206.6(VPS35):c.505G>C (p.Asp169His)
NM_018206.6(VPS35):c.648G>A (p.Leu216=)
NM_018206.6(VPS35):c.851G>A (p.Arg284Gln) rs771276024
NM_018206.6(VPS35):c.89T>A (p.Met30Lys) rs145147781

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