List of variants in gene XIAP reported as benign for Lymphoproliferative 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001167.4(XIAP):c.*5505del	rs111508332	0.24545
NM_001167.4(XIAP):c.5068_5069insT	rs58114044	0.15926
NM_001167.4(XIAP):c.2296_2300del	rs79291374
NM_001167.4(XIAP):c.*3702dup	rs762141177
NM_001167.4(XIAP):c.*4309dup	rs397713705
NM_001167.4(XIAP):c.*5047del	rs368295939
NM_001167.4(XIAP):c.*5180del	rs60841987
NM_001167.4(XIAP):c.*5180dup	rs60841987
NM_001167.4(XIAP):c.*5519del	rs374013599

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