ClinVar Miner

List of variants in gene SYNJ1 reported as likely benign for Parkinson disease

Included ClinVar conditions (32):
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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_003895.3(SYNJ1):c.1026A>G (p.Gly342=) rs145522240
NM_003895.3(SYNJ1):c.1147G>A (p.Ala383Thr) rs114942253
NM_003895.3(SYNJ1):c.1652C>T (p.Ala551Val) rs115989459
NM_003895.3(SYNJ1):c.1947C>G (p.Leu649=) rs115658799
NM_003895.3(SYNJ1):c.2023G>A (p.Val675Ile) rs373820739
NM_003895.3(SYNJ1):c.210C>G (p.Leu70=) rs201322530
NM_003895.3(SYNJ1):c.2463G>A (p.Pro821=) rs61753644
NM_003895.3(SYNJ1):c.2992-5G>A rs376206541
NM_003895.3(SYNJ1):c.3114T>C (p.Leu1038=) rs111774827
NM_003895.3(SYNJ1):c.3322A>G (p.Ser1108Gly) rs149817769
NM_003895.3(SYNJ1):c.3707C>T (p.Thr1236Met) rs145937537
NM_003895.3(SYNJ1):c.4033G>A (p.Val1345Ile) rs115648918
NM_003895.3(SYNJ1):c.4252A>G (p.Ile1418Val) rs113978322
NM_003895.3(SYNJ1):c.4341C>T (p.Asp1447=) rs149199429
NM_003895.3(SYNJ1):c.4551G>A (p.Pro1517=) rs777945782
NM_003895.3(SYNJ1):c.4581G>A (p.Glu1527=) rs146425050
NM_003895.3(SYNJ1):c.4757C>T (p.Pro1586Leu) rs2230767
NM_003895.3(SYNJ1):c.4790C>T (p.Thr1597Met) rs111516740
NM_003895.3(SYNJ1):c.538T>C (p.Leu180=) rs140461566
NM_003895.3(SYNJ1):c.960T>C (p.Ala320=) rs372016074
NM_203446.2(SYNJ1):c.*234G>T rs777299829
NM_203446.2(SYNJ1):c.*738C>T rs747245690
NM_203446.2(SYNJ1):c.1119C>T (p.Asp373=) rs763601982
NM_203446.2(SYNJ1):c.2263-8G>A rs759701632
NM_203446.2(SYNJ1):c.2703C>T (p.Val901=) rs771973400
NM_203446.2(SYNJ1):c.282A>G (p.Lys94=) rs141138675
NM_203446.2(SYNJ1):c.2961C>T (p.Ala987=) rs1432339434
NM_203446.2(SYNJ1):c.3402G>A (p.Pro1134=) rs376395608
NM_203446.2(SYNJ1):c.3753G>A (p.Ala1251=) rs576444776
NM_203446.2(SYNJ1):c.3864G>T (p.Pro1288=) rs138579227
NM_203446.2(SYNJ1):c.3879C>T (p.Pro1293=) rs201117151
NM_203446.2(SYNJ1):c.4029G>A (p.Pro1343=) rs372695378

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