List of variants in gene LOC130066606, RUNX1 studied 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
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.58+264C>T	rs9981811	0.07034
NM_001754.5(RUNX1):c.58+265G>A	rs73900787	0.05102

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