List of variants in gene combination LOC107985033, SLFN14 reported as benign for hematologic disorder

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001129820.2(SLFN14):c.1153A>G (p.Lys385Glu)	rs321612	0.64723
NM_001129820.2(SLFN14):c.1066C>T (p.Pro356Ser)	rs321613	0.64716
NM_001129820.2(SLFN14):c.1061-11T>C	rs321614	0.46920
NM_001129820.2(SLFN14):c.1348A>G (p.Lys450Glu)	rs79007502	0.02530

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