ClinVar Miner

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

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_003895.3(SYNJ1):c.1236-8G>T rs138882423
NM_003895.3(SYNJ1):c.123G>A (p.Ala41=) rs61750221
NM_003895.3(SYNJ1):c.160C>T (p.Pro54Ser) rs61755328
NM_003895.3(SYNJ1):c.1663G>A (p.Val555Ile) rs113708828
NM_003895.3(SYNJ1):c.2031G>A (p.Leu677=) rs534908601
NM_003895.3(SYNJ1):c.2343T>A (p.Val781=) rs566533509
NM_003895.3(SYNJ1):c.3060G>T (p.Met1020Ile) rs115683257
NM_003895.3(SYNJ1):c.3486A>G (p.Pro1162=) rs368850131
NM_003895.3(SYNJ1):c.4032+5G>T rs61750220
NM_003895.3(SYNJ1):c.4215_4216insAATAC (p.Leu1406fs) rs869265580
NM_003895.3(SYNJ1):c.4344G>A (p.Arg1448=) rs145347648
NM_003895.3(SYNJ1):c.4358G>A (p.Gly1453Glu) rs61750217
NM_003895.3(SYNJ1):c.4640C>T (p.Pro1547Leu) rs76056543
NM_003895.3(SYNJ1):c.596+9A>G rs76502784
NM_003895.3(SYNJ1):c.690A>G (p.Thr230=) rs61756694
NM_003895.3(SYNJ1):c.822+7A>G rs187016397
NM_003895.3(SYNJ1):c.823-15dup rs202044634

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