List of variants in gene combination NKIRAS1, RPL15 reported as uncertain significance for aplastic anemia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002948.5(RPL15):c.458A>G (p.Lys153Arg)	rs370700905	0.00005
NM_002948.5(RPL15):c.172+5G>A	rs369956511	0.00004
NM_002948.5(RPL15):c.536A>G (p.Lys179Arg)	rs774572575	0.00001

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