List of variants in gene KNL1 reported as benign by Genetic Services Laboratory, University of Chicago

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_144508.5(KNL1):c.259A>G (p.Thr87Ala)	rs12911738	0.83758
NM_144508.5(KNL1):c.1378G>T (p.Ala460Ser)	rs2412541	0.79293
NM_144508.5(KNL1):c.128G>C (p.Arg43Thr)	rs7177192	0.79283
NM_144508.5(KNL1):c.3432T>C (p.Asn1144=)	rs11070285	0.39065
NM_144508.5(KNL1):c.1715T>C (p.Met572Thr)	rs11858113	0.39038
NM_144508.5(KNL1):c.2583T>G (p.Thr861=)	rs8041534	0.38951
NM_144508.5(KNL1):c.2310C>T (p.Val770=)	rs11855334	0.38914
NM_144508.5(KNL1):c.3775A>G (p.Lys1259Glu)	rs17747633	0.30695
NM_144508.5(KNL1):c.250+556G>A	rs8030491	0.03326
NM_144508.5(KNL1):c.727A>G (p.Ile243Val)	rs76371152	0.01510
NM_144508.5(KNL1):c.4931A>G (p.Lys1644Arg)	rs76098847	0.01498
NM_144508.5(KNL1):c.3810G>A (p.Ala1270=)	rs34758606	0.00949
NM_144508.5(KNL1):c.4170T>A (p.Asp1390Glu)	rs141726041	0.00141

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