List of variants in gene XIAP reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_001167.4(XIAP):c.*1904G>A	rs751700391	0.00118
NM_001167.4(XIAP):c.*870G>C	rs185823003	0.00084
NM_001167.4(XIAP):c.*2521A>G	rs746553843	0.00046
NM_001167.4(XIAP):c.*6220C>T	rs370656891	0.00037
NM_001167.4(XIAP):c.*3408G>T	rs746713249	0.00035
NM_001167.4(XIAP):c.*6010G>A	rs764617684	0.00027
NM_001167.4(XIAP):c.*3544G>A	rs747125911	0.00025
NM_001167.4(XIAP):c.*1705A>G	rs766498412	0.00018
NM_001167.4(XIAP):c.*1481C>T	rs1483818489	0.00011
NM_001167.4(XIAP):c.*1940T>C	rs755490620	0.00009
NM_001167.4(XIAP):c.*6221G>A	rs757596272	0.00009
NM_001167.4(XIAP):c.*3001T>A	rs765082277	0.00008
NM_001167.4(XIAP):c.*2488C>T	rs1192771463	0.00003
NM_001167.4(XIAP):c.*253C>T	rs1057515749	0.00003
NM_001167.4(XIAP):c.*3845A>G	rs958117071	0.00003
NM_001167.4(XIAP):c.*4691G>A	rs982138652	0.00002
NM_001167.4(XIAP):c.-142G>C	rs1452980309	0.00002
NM_001167.4(XIAP):c.*1869G>A	rs1225539193	0.00001
NM_001167.4(XIAP):c.*1950C>T	rs1404651190	0.00001
NM_001167.4(XIAP):c.*3205T>C	rs777738703	0.00001
NM_001167.4(XIAP):c.*3673C>T	rs1304742588	0.00001
NM_001167.4(XIAP):c.*3997A>G	rs1057515755	0.00001
NM_001167.4(XIAP):c.*5986G>A	rs1037241174	0.00001
NM_001167.4(XIAP):c.*6009C>T	rs1183404777	0.00001
NM_001167.4(XIAP):c.*6256T>C	rs972613558	0.00001
NM_001167.4(XIAP):c.*2401C>T	rs771727226
NM_001167.4(XIAP):c.*2901T>C	rs1057515751
NM_001167.4(XIAP):c.*3201A>G	rs1057515752
NM_001167.4(XIAP):c.*3547C>G	rs775436856
NM_001167.4(XIAP):c.*3573G>A	rs1037858715
NM_001167.4(XIAP):c.*3589A>C	rs2053592868
NM_001167.4(XIAP):c.4307_4309dup	rs397713705
NM_001167.4(XIAP):c.*4336T>G	rs2053603008
NM_001167.4(XIAP):c.*5047dup	rs368295939
NM_001167.4(XIAP):c.*5070del	rs751242607
NM_001167.4(XIAP):c.*5180dup	rs60841987
NM_001167.4(XIAP):c.*6211C>T	rs1022688672
NM_001167.4(XIAP):c.*6216G>A	rs1057515760
NM_001167.4(XIAP):c.*866A>G	rs2053568767
NM_001167.4(XIAP):c.*93T>G	rs2053562277
NM_001167.4(XIAP):c.1237G>A (p.Asp413Asn)	rs199610221
NM_001167.4(XIAP):c.1317G>C (p.Glu439Asp)	rs2053559883

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