List of variants in gene ICOS reported as benign for common variable immunodeficiency

Minimum submission review status:		Collection method:
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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_012092.4(ICOS):c.587-26T>G	rs10172036	0.57656
NM_012092.4(ICOS):c.*2A>C	rs10183087	0.29378
NM_012092.4(ICOS):c.*964T>C	rs4404254	0.29332
NM_012092.4(ICOS):c.*1407G>A	rs1559931	0.29190
NM_012092.4(ICOS):c.*1773G>C	rs4675379	0.14872
NM_012092.4(ICOS):c.*1262A>G	rs10932038	0.08229
NM_012092.4(ICOS):c.*859A>T	rs10932036	0.08225
NM_012092.4(ICOS):c.*330G>A	rs10932035	0.08223
NM_012092.4(ICOS):c.*1024C>T	rs10932037	0.08219
NM_012092.4(ICOS):c.*33T>C	rs73058105	0.03775
NM_012092.4(ICOS):c.*1095A>G	rs73991307	0.02660
NM_012092.4(ICOS):c.*855T>C	rs73991306	0.02657
NM_012092.4(ICOS):c.150A>G (p.Gln50=)	rs55972840	0.02252
NM_012092.4(ICOS):c.501+7G>A	rs57149344	0.02252
NM_012092.4(ICOS):c.*1249G>A	rs73991308	0.02203
NM_012092.4(ICOS):c.40C>T (p.Arg14Cys)	rs77411896	0.00783
NM_012092.4(ICOS):c.58+9T>G	rs140049646	0.00348
NM_012092.4(ICOS):c.375A>G (p.Gly125=)	rs768500706	0.00064
NM_012092.4(ICOS):c.591G>A (p.Val197=)	rs55655222	0.00012
NM_012092.4(ICOS):c.395-10dup	rs750240095
NM_012092.4(ICOS):c.501+6C>T	rs4264550

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