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

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_020661.4(AICDA):c.*1139A>G	rs773190855	0.00330
NM_020661.4(AICDA):c.299G>C (p.Gly100Ala)	rs201210527	0.00138
NM_020661.4(AICDA):c.427+4C>T	rs201180477	0.00130
NM_020661.4(AICDA):c.*958A>G	rs184392902	0.00053
NM_020661.4(AICDA):c.*1934C>T	rs104894981	0.00035
NM_020661.4(AICDA):c.*1662C>A	rs527675973	0.00022
NM_020661.4(AICDA):c.*1704C>T	rs557005026	0.00020
NM_020661.4(AICDA):c.*470C>G	rs190321240

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