List of variants in gene combination GATA3, LOC130003278 reported as benign for chromosomal 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001002295.2(GATA3):c.241+8C>T	rs376505863	0.00009
NM_001002295.2(GATA3):c.216G>T (p.Val72=)	rs560531559	0.00006

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