List of variants in gene AICDA reported as benign for B cell deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_020661.4(AICDA):c.-84A>G	rs1345004	0.99525
NM_020661.4(AICDA):c.156+16G>A	rs2518144	0.55804
NM_020661.4(AICDA):c.465C>T (p.His155=)	rs2028373	0.53597
NM_020661.4(AICDA):c.*89A>C	rs11046349	0.23977
NM_020661.4(AICDA):c.*309T>C	rs12307097	0.11052
NM_020661.4(AICDA):c.*1028C>T	rs7304723	0.09017
NM_020661.4(AICDA):c.*1297G>A	rs140765460	0.03904
NM_020661.4(AICDA):c.*1694A>G	rs75351379	0.02262
NM_020661.4(AICDA):c.*1666G>T	rs115523544	0.01479
NM_020661.4(AICDA):c.*1206C>T	rs147762245	0.01472
NM_020661.4(AICDA):c.*718C>A	rs74372815	0.01333
NM_020661.4(AICDA):c.210A>G (p.Leu70=)	rs104894984	0.00916
NM_020661.4(AICDA):c.585T>C (p.Thr195=)	rs78590060	0.00370
NM_020661.4(AICDA):c.267C>T (p.Asp89=)	rs74334270	0.00326
NM_020661.4(AICDA):c.74G>A (p.Arg25His)	rs61730095	0.00289
NM_020661.4(AICDA):c.428-18C>T	rs201393772	0.00235
NM_020661.4(AICDA):c.369C>T (p.Pro123=)	rs199980715	0.00171
NM_020661.4(AICDA):c.*1089C>T	rs141460280	0.00097
NM_020661.4(AICDA):c.*38T>C	rs115089086
NM_020661.4(AICDA):c.428-17_428-16dup	rs5796316
NM_020661.4(AICDA):c.428-17dup	rs5796316

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