List of variants in gene KL reported as likely 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_004795.4(KL):c.1593C>T (p.Tyr531=)	rs62637617	0.03076
NM_004795.4(KL):c.*510C>T	rs77813367	0.01271
NM_004795.4(KL):c.*1664T>C	rs116627995	0.01270
NM_004795.4(KL):c.*1455A>G	rs77174048	0.01269
NM_004795.4(KL):c.*407T>C	rs75520088	0.01175
NM_004795.4(KL):c.*722T>C	rs183407162	0.01088
NM_004795.4(KL):c.595C>T (p.Arg199Cys)	rs200063460	0.00849
NM_004795.4(KL):c.*1347C>G	rs556051453	0.00143
NM_004795.4(KL):c.2532G>A (p.Gln844=)	rs149775738	0.00111
NM_004795.4(KL):c.*32A>G	rs373955636	0.00071
NM_004795.4(KL):c.614G>A (p.Gly205Asp)	rs200611452	0.00026
NM_004795.4(KL):c.387C>T (p.Tyr129=)	rs373385333	0.00021
NM_004795.4(KL):c.*1766T>G	rs568662502
NM_004795.4(KL):c.2296G>A (p.Gly766Ser)	rs114752661

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