ClinVar Miner

List of variants studied for Parkinson disease 17 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 38
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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.*289C>T
NM_018206.6(VPS35):c.*345T>G
NM_018206.6(VPS35):c.*346G>A rs545755034
NM_018206.6(VPS35):c.*34A>G
NM_018206.6(VPS35):c.*354G>C rs572048744
NM_018206.6(VPS35):c.*380G>A rs886052004
NM_018206.6(VPS35):c.*401G>A rs553790361
NM_018206.6(VPS35):c.*422C>A
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.-34G>A rs3743928
NM_018206.6(VPS35):c.-35C>G
NM_018206.6(VPS35):c.-35C>T rs189775907
NM_018206.6(VPS35):c.1035G>A (p.Glu345=) rs563975281
NM_018206.6(VPS35):c.1145A>G (p.Lys382Arg) rs116254156
NM_018206.6(VPS35):c.1268C>T (p.Pro423Leu)
NM_018206.6(VPS35):c.1317T>C (p.Tyr439=)
NM_018206.6(VPS35):c.1420C>G (p.Gln474Glu) rs370401767
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.2145A>G (p.Leu715=) rs145033509
NM_018206.6(VPS35):c.2211+11T>C
NM_018206.6(VPS35):c.2241C>T (p.Ile747=) rs140543776
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.678C>T (p.Arg226=) rs376845827
NM_018206.6(VPS35):c.851G>A (p.Arg284Gln) rs771276024
NM_018206.6(VPS35):c.89T>A (p.Met30Lys) rs145147781
NM_018206.6(VPS35):c.945A>T (p.Gly315=) rs144346159

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