List of variants in gene EXOSC9 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_005033.3(EXOSC9):c.827+73A>G	rs4295291	0.79272
NM_005033.3(EXOSC9):c.1156+24_1156+26dup	rs59269603	0.78639
NM_005033.3(EXOSC9):c.161+30G>A	rs67772833	0.49185
NM_005033.3(EXOSC9):c.66+48C>G	rs3811742	0.31224
NM_005033.3(EXOSC9):c.605+188A>T	rs9998785	0.29313
NC_000004.12:g.121801213G>A	rs3828485	0.27394
NM_005033.3(EXOSC9):c.1096A>G (p.Ile366Val)	rs1803183	0.08928
NM_005033.3(EXOSC9):c.1157-52C>T	rs1507988	0.06734
NM_005033.3(EXOSC9):c.828-11C>T	rs3811743	0.06544
NM_005033.3(EXOSC9):c.522+115A>G	rs72680748	0.03922
NM_005033.3(EXOSC9):c.282-17C>T	rs34669312	0.03844
NM_005033.3(EXOSC9):c.-47G>A	rs115766017	0.01728
NM_005033.3(EXOSC9):c.385-185C>T	rs41505154	0.01725
NM_005033.3(EXOSC9):c.975-53A>G	rs4256243	0.01725
NM_005033.3(EXOSC9):c.1156+22_1156+23insTTT	rs200440088	0.01646
NM_005033.3(EXOSC9):c.66+51A>C	rs57880593	0.01574
NM_005033.3(EXOSC9):c.827+17G>A	rs17452087	0.01179
NM_005033.3(EXOSC9):c.385-14A>G	rs150388479	0.00726
NM_005033.3(EXOSC9):c.1086T>C (p.Gly362=)	rs76155182	0.00607
NM_005033.3(EXOSC9):c.1156+23C>A	rs75746413	0.00578
NM_005033.3(EXOSC9):c.523-35_523-19del	rs533338101	0.00274
NM_005033.3(EXOSC9):c.66+15C>T	rs139419769	0.00138
NM_005033.3(EXOSC9):c.552A>G (p.Pro184=)	rs202243579	0.00009
NM_005033.3(EXOSC9):c.997A>C (p.Thr333Pro)	rs533678536	0.00002
NM_005033.3(EXOSC9):c.1157-12A>G
NM_005033.3(EXOSC9):c.1157-21del	rs35942869
NM_005033.3(EXOSC9):c.1157-21dup	rs35942869
NM_005033.3(EXOSC9):c.1157-6dup
NM_005033.3(EXOSC9):c.522+159C>T	rs6836544
NM_005033.3(EXOSC9):c.523-13del
NM_005033.3(EXOSC9):c.915C>T (p.Thr305=)

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