List of variants in gene combination LOC130060889, STAT3 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.594G>C (p.Gln198His)	rs374063766	0.00001
NM_139276.3(STAT3):c.571A>C (p.Asn191His)
NM_139276.3(STAT3):c.576C>G (p.Asn192Lys)
NM_139276.3(STAT3):c.579G>C (p.Gln193His)
NM_139276.3(STAT3):c.586_590dup (p.Gln198fs)

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