List of variants in gene LAMTOR2 reported as uncertain significance for leukopenia

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014017.4(LAMTOR2):c.231+7A>G	rs750943723	0.00002
NM_014017.4(LAMTOR2):c.47C>T (p.Thr16Ile)	rs763874836	0.00001

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