List of variants reported as uncertain significance for Hyper-IgM syndrome type 2 by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_020661.4(AICDA):c.*1137A>G	rs867594346	0.05656
NM_020661.4(AICDA):c.*1136A>G	rs371020938	0.03107
NM_020661.4(AICDA):c.*446G>A	rs104894982	0.00275
NM_020661.4(AICDA):c.48A>G (p.Lys16=)	rs186739900	0.00117
NM_020661.4(AICDA):c.*67C>T	rs149095678	0.00081
NM_020661.4(AICDA):c.*1213A>G	rs751259274	0.00045
NM_020661.4(AICDA):c.*235C>G	rs112610523	0.00037
NM_020661.4(AICDA):c.*625T>C	rs112850229	0.00036
NM_020661.4(AICDA):c.*1173C>T	rs192088951	0.00017
NM_020661.4(AICDA):c.*554T>C	rs886049874	0.00016
NM_020661.4(AICDA):c.*771T>A	rs1189292106	0.00014
NM_020661.4(AICDA):c.*670A>T	rs886049873	0.00013
NM_020661.4(AICDA):c.*1010C>T	rs1018192148	0.00006
NM_020661.4(AICDA):c.*1296C>T	rs748400078	0.00004
NM_020661.4(AICDA):c.*1684T>C	rs1026369274	0.00004
NM_020661.4(AICDA):c.376C>T (p.Leu126=)	rs999930122	0.00002
NM_020661.4(AICDA):c.569G>A (p.Arg190Gln)	rs747680644	0.00002
NM_020661.4(AICDA):c.*1025G>A	rs1941216576	0.00001
NM_020661.4(AICDA):c.-87A>T	rs1941389378	0.00001
NM_020661.4(AICDA):c.29A>G (p.Lys10Arg)	rs768249578	0.00001
NM_020661.4(AICDA):c.*1083T>C	rs886049870
NM_020661.4(AICDA):c.*1106A>G	rs886049869
NM_020661.4(AICDA):c.*1138A>G	rs7138990
NM_020661.4(AICDA):c.*1226A>C	rs887527114
NM_020661.4(AICDA):c.*1262C>T	rs886049868
NM_020661.4(AICDA):c.*1313G>C	rs1941208167
NM_020661.4(AICDA):c.*1380A>G	rs1286233476
NM_020661.4(AICDA):c.*1453A>G	rs1188858698
NM_020661.4(AICDA):c.*1455G>A	rs187473552
NM_020661.4(AICDA):c.*1802T>C	rs1941199404
NM_020661.4(AICDA):c.*288C>T	rs886049875
NM_020661.4(AICDA):c.*38T>G	rs115089086
NM_020661.4(AICDA):c.*556T>G	rs3205190
NM_020661.4(AICDA):c.*804A>T	rs886049872
NM_020661.4(AICDA):c.*837A>G	rs886049871

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