List of variants in gene LILRB3 reported as likely benign

Minimum submission review status:		Collection method:
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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_006864.4(LILRB3):c.418A>G (p.Met140Val)	rs544847770	0.00016
NM_006864.4(LILRB3):c.1192G>A (p.Gly398Ser)	rs781128474	0.00004
NM_006864.4(LILRB3):c.1522G>A (p.Val508Ile)	rs372186200	0.00004
NM_006864.4(LILRB3):c.1357G>A (p.Val453Ile)	rs572753215	0.00002
NM_006864.4(LILRB3):c.1112T>A (p.Met371Lys)
NM_006864.4(LILRB3):c.1572C>G (p.Asp524Glu)	rs200450535
NM_006864.4(LILRB3):c.330C>T (p.Ser110=)
NM_006864.4(LILRB3):c.411G>A (p.Gly137=)
NM_006864.4(LILRB3):c.870= (p.Tyr290=)

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