List of variants in gene PIGL reported as benign for CHIME syndrome

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004278.4(PIGL):c.*20A>G	rs15739	0.39527
NM_004278.4(PIGL):c.*86A>G	rs2302314	0.06241
NM_004278.4(PIGL):c.*364G>A	rs114659268	0.00706
NM_004278.4(PIGL):c.*182A>G	rs140126036	0.00231
NM_004278.4(PIGL):c.526+10G>A	rs138410893	0.00121

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