List of variants in gene combination HOXA11, LOC107126281 reported as uncertain significance for hematologic disorder

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_005523.6(HOXA11):c.396G>C (p.Arg132Ser)	rs143812636	0.00052
NM_005523.6(HOXA11):c.248A>G (p.Tyr83Cys)	rs778467438	0.00001
NM_005523.6(HOXA11):c.451C>A (p.Pro151Thr)

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