List of variants in gene combination LOC129936399, TGFBR2 reported as likely benign for retinal 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_003242.6(TGFBR2):c.-128C>G	rs2306856	0.10667
NM_003242.6(TGFBR2):c.-117G>A	rs886058302	0.00001
NM_003242.6(TGFBR2):c.-122T>G	rs1040386724

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