List of variants in gene SYNJ1 studied for Early-onset Parkinson disease 20

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_203446.3(SYNJ1):c.3518-7G>T	rs2833929	0.28042
NM_203446.3(SYNJ1):c.1906G>A (p.Val636Ile)	rs373820739	0.00007
NM_203446.3(SYNJ1):c.-56G>T	rs1486511197	0.00001
NM_203446.3(SYNJ1):c.1318T>C (p.Tyr440His)	rs1454342974	0.00001
NM_203446.3(SYNJ1):c.3601C>T (p.Arg1201Cys)	rs114994257	0.00001
NM_203446.3(SYNJ1):c.656G>A (p.Arg219Gln)	rs398122403	0.00001
NM_203446.3(SYNJ1):c.186_187insAATACT	rs57257560
NM_203446.3(SYNJ1):c.1001A>G (p.Asp334Gly)	rs2146090425
NM_203446.3(SYNJ1):c.1259G>C (p.Arg420Pro)	rs1060499619
NM_203446.3(SYNJ1):c.1646G>A (p.Arg549His)	rs1363168296
NM_203446.3(SYNJ1):c.2242C>T (p.Gln748Ter)
NM_203446.3(SYNJ1):c.2254del (p.Asp752fs)	rs2040866242
NM_203446.3(SYNJ1):c.2398C>T (p.Arg800Cys)
NM_203446.3(SYNJ1):c.319C>T (p.Arg107Ter)
NM_203446.3(SYNJ1):c.3394G>T (p.Ala1132Ser)
NM_203446.3(SYNJ1):c.395G>A (p.Trp132Ter)	rs1555907463
NM_203446.3(SYNJ1):c.577T>C (p.Tyr193His)	rs2042158818

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