List of variants in gene combination LOC130060888, STAT3 reported as benign 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_139276.3(STAT3):c.711C>T (p.Asp237=)	rs17882069	0.00712
NM_139276.3(STAT3):c.666G>A (p.Ala222=)
NM_139276.3(STAT3):c.708G>A (p.Thr236=)

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