List of variants in gene combination CHRNG, TIGD1 reported as benign for primary lymphedema

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_005199.5(CHRNG):c.*568C>T	rs72991939	0.18562
NM_005199.5(CHRNG):c.*496A>G	rs72991937	0.18514
NM_005199.5(CHRNG):c.1422C>T (p.Arg474=)	rs2099489	0.17611

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