List of variants in gene combination KANSL1, MAPT reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015443.4(KANSL1):c.3029C>T (p.Pro1010Leu)	rs7220988	0.34127
NM_015443.4(KANSL1):c.3254T>C (p.Ile1085Thr)	rs34579536	0.14468
NM_015443.4(KANSL1):c.2742C>T (p.Asp914=)	rs35833914	0.14434
NM_015443.4(KANSL1):c.2751C>T (p.Phe917=)	rs36076725	0.14426

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