Variants in gene COG7 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

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HGVS	dbSNP	gnomAD frequency
NM_153603.4(COG7):c.1178A>G (p.His393Arg)	rs116331296	0.00233
NM_153603.4(COG7):c.850A>T (p.Ile284Phe)	rs115605801	0.00094
NM_153603.4(COG7):c.1455C>T (p.Phe485=)	rs116153163	0.00068
NM_153603.4(COG7):c.2052G>A (p.Ser684=)	rs142744907	0.00060
NM_153603.4(COG7):c.1972G>A (p.Ala658Thr)	rs115073082	0.00014
NM_153603.4(COG7):c.904G>A (p.Val302Met)	rs116314856	0.00014
NM_153603.4(COG7):c.2013G>A (p.Leu671=)	rs370447404	0.00012
NM_153603.4(COG7):c.1851C>T (p.Pro617=)	rs748835759	0.00006
NM_153603.4(COG7):c.1137+9G>A	rs746762111	0.00004
NM_153603.4(COG7):c.963C>T (p.Thr321=)	rs762510375	0.00004
NM_153603.4(COG7):c.1167G>A (p.Gln389=)	rs201313774	0.00003
NM_153603.4(COG7):c.1410-6G>C	rs369925503	0.00003
NM_153603.4(COG7):c.1629T>C (p.Tyr543=)	rs760342154	0.00003
NM_153603.4(COG7):c.1804-13G>A	rs759680428	0.00003
NM_153603.4(COG7):c.687+14C>T	rs139853094	0.00001
NM_153603.4(COG7):c.1005C>T (p.His335=)	rs532636981
NM_153603.4(COG7):c.1305T>C (p.Asp435=)	rs1019861391

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