List of variants in gene SYNJ1 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_203446.3(SYNJ1):c.3479-300_3479-299insAA	rs10662219	0.99232
NM_203446.3(SYNJ1):c.479+255A>C	rs1783099	0.57104
NM_203446.3(SYNJ1):c.948+81G>A	rs844975	0.56967
NM_203446.3(SYNJ1):c.3391+99A>T	rs2406	0.55662
NM_203446.3(SYNJ1):c.3247+266G>A	rs844978	0.55052
NM_203446.3(SYNJ1):c.2145+140A>T	rs701734	0.53198
NM_203446.3(SYNJ1):c.1510+15del	rs201012663	0.46240
NM_203446.3(SYNJ1):c.884A>G (p.Lys295Arg)	rs2254562	0.29094
NM_203446.3(SYNJ1):c.3518-7G>T	rs2833929	0.28042
NM_203446.3(SYNJ1):c.3588+14C>T	rs11702774	0.16837
NM_203446.3(SYNJ1):c.1201-3A>T	rs844988	0.08382
NM_203446.3(SYNJ1):c.1812-100T>C	rs844998	0.08158
NM_203446.3(SYNJ1):c.*3+254A>C	rs844985	0.08067
NM_203446.3(SYNJ1):c.3721C>T (p.Leu1241=)	rs2230766	0.07370
NM_203446.3(SYNJ1):c.-23+128C>T	rs117275928	0.06596
NM_203446.3(SYNJ1):c.479+9A>G	rs76502784	0.03297
NM_203446.3(SYNJ1):c.1511-59T>A	rs116389986	0.01650
NM_203446.3(SYNJ1):c.3915+5G>T	rs61750220	0.01369
NM_203446.3(SYNJ1):c.*329G>A	rs61750217	0.00954
NM_203446.3(SYNJ1):c.*611C>T	rs76056543	0.00609
NM_203446.3(SYNJ1):c.1119-8G>T	rs138882423	0.00462
NM_203446.3(SYNJ1):c.6G>A (p.Ala2=)	rs61750221	0.00452
NM_203446.3(SYNJ1):c.43C>T (p.Pro15Ser)	rs61755328	0.00441
NM_203446.3(SYNJ1):c.573A>G (p.Thr191=)	rs61756694	0.00406
NM_203446.3(SYNJ1):c.705+7A>G	rs187016397	0.00040
NM_203446.3(SYNJ1):c.186_187insAATACT	rs57257560
NM_203446.3(SYNJ1):c.-23+157dup	rs35924673
NM_203446.3(SYNJ1):c.1200+55T>C	rs75924460
NM_203446.3(SYNJ1):c.2305-110T>A	rs2833936
NM_203446.3(SYNJ1):c.2461+245T>C	rs762227
NM_203446.3(SYNJ1):c.3479-18del	rs555916409

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