Variants in gene STAT3 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_139276.3(STAT3):c.1003C>T (p.Arg335Trp)	rs193922716
NM_139276.3(STAT3):c.1261G>A (p.Gly421Arg)	rs869312888
NM_139276.3(STAT3):c.1970A>G (p.Tyr657Cys)	rs193922721
NM_139276.3(STAT3):c.1976T>A (p.Ile659Asn)	rs1555563717
NM_139276.3(STAT3):c.2144C>T (p.Pro715Leu)	rs1064794957
NM_139276.3(STAT3):c.994C>T (p.His332Tyr)	rs2144827923

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