List of variants in gene IL16 reported as likely benign

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_172217.5(IL16):c.2199T>C (p.His733=)	rs146704319	0.00054
NM_172217.5(IL16):c.3546C>A (p.Leu1182=)	rs150362407	0.00040
NM_172217.5(IL16):c.911C>T (p.Thr304Met)	rs537866391	0.00011
NM_172217.5(IL16):c.1993A>G (p.Ile665Val)	rs541690334	0.00003
NM_172217.5(IL16):c.1975G>A (p.Gly659Ser)	rs199946459	0.00001
NM_172217.5(IL16):c.19G>A (p.Ala7Thr)	rs750324638	0.00001
NM_172217.5(IL16):c.2592C>G (p.Leu864=)	rs1046094990	0.00001
NM_172217.5(IL16):c.1200G>C (p.Arg400=)
NM_172217.5(IL16):c.1903-5C>A	rs759090105
NM_172217.5(IL16):c.2222A>G (p.Asn741Ser)
NM_172217.5(IL16):c.2780G>A (p.Arg927Gln)
NM_172217.5(IL16):c.300A>G (p.Ile100Met)
NM_172217.5(IL16):c.3832G>A (p.Val1278Ile)
NM_172217.5(IL16):c.563C>T (p.Ala188Val)

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