List of variants in gene combination LOC130060888, STAT3 reported as likely 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.681G>A (p.Ala227=)	rs775680553	0.00016
NM_139276.3(STAT3):c.690C>T (p.Tyr230=)	rs746151758	0.00003
NM_139276.3(STAT3):c.646-7C>T	rs993067731	0.00001
NM_139276.3(STAT3):c.651C>T (p.Ile217=)	rs377095381	0.00001
NM_139276.3(STAT3):c.657T>C (p.Ser219=)	rs886052943	0.00001
NM_139276.3(STAT3):c.746T>C (p.Ile249Thr)	rs767159289	0.00001
NM_139276.3(STAT3):c.646-13G>T
NM_139276.3(STAT3):c.646-8C>A
NM_139276.3(STAT3):c.652G>C (p.Val218Leu)
NM_139276.3(STAT3):c.708G>C (p.Thr236=)	rs1007672644
NM_139276.3(STAT3):c.720G>A (p.Leu240=)
NM_139276.3(STAT3):c.750C>T (p.Ala250=)
NM_139276.3(STAT3):c.765G>A (p.Pro255=)
NM_139276.3(STAT3):c.797+13A>G
NM_139276.3(STAT3):c.797+17G>A
NM_139276.3(STAT3):c.797+18C>T

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