List of variants in gene combination LOC129997366, STX11 reported as uncertain significance for lymphatic system 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_003764.4(STX11):c.-140C>T	rs886061139	0.00001
NM_003764.4(STX11):c.-125C>G	rs1055093473
NM_003764.4(STX11):c.-71C>T	rs886061140

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