List of variants in gene combination KANSL1, MAPT reported as benign by Illumina Laboratory Services, Illumina

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.1145_1146insT	rs1491446284	0.40313
NM_015443.4(KANSL1):c.3029C>T (p.Pro1010Leu)	rs7220988	0.34127
NM_001377265.1(MAPT):c.*1101A>G	rs1052590	0.14499
NM_001377265.1(MAPT):c.*1759T>C	rs7687	0.14487
NM_015443.4(KANSL1):c.*487C>T	rs17652961	0.14478
NM_001377265.1(MAPT):c.*2806A>C	rs2158257	0.14473
NM_001377265.1(MAPT):c.*1067T>C	rs1052587	0.14468
NM_015443.4(KANSL1):c.3254T>C (p.Ile1085Thr)	rs34579536	0.14468
NM_001377265.1(MAPT):c.*2972T>C	rs17574228	0.14466
NM_015443.4(KANSL1):c.*640T>C	rs17574361	0.14457
NM_001377265.1(MAPT):c.*2079C>T	rs17652748	0.14441
NM_015443.4(KANSL1):c.2742C>T (p.Asp914=)	rs35833914	0.14434
NM_015443.4(KANSL1):c.2751C>T (p.Phe917=)	rs36076725	0.14426
NM_015443.4(KANSL1):c.*742G>A	rs7350928	0.12614
NM_001377265.1(MAPT):c.*1152G>C	rs1052594	0.12578
NM_001377265.1(MAPT):c.*2269G>T	rs73317039	0.03265
NM_001377265.1(MAPT):c.*3848A>G	rs114213384	0.03189
NM_001377265.1(MAPT):c.*1047C>T	rs113815715	0.02477
NM_001377265.1(MAPT):c.*2810G>A	rs2158256	0.02237
NM_001377265.1(MAPT):c.*3078=
NM_015443.4(KANSL1):c.*1235dup	rs140510364
NM_015443.4(KANSL1):c.*1328del	rs71665335
NM_015443.4(KANSL1):c.*1354del	rs67641084
NM_015443.4(KANSL1):c.*1520del	rs67801660
NM_015443.4(KANSL1):c.359_360insAGAGGGC	rs113448888
NM_015443.4(KANSL1):c.*885del	rs5820607

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