List of variants in gene CARD9 reported as benign for Predisposition to invasive fungal disease due to CARD9 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_052813.5(CARD9):c.126C>T (p.Pro42=)	rs10781499	0.38097
NM_052813.5(CARD9):c.35G>A (p.Ser12Asn)	rs4077515	0.38018
NM_052813.5(CARD9):c.228C>T (p.Tyr76=)	rs11145769	0.03984
NM_052813.5(CARD9):c.693G>A (p.Thr231=)	rs59902911	0.03899
NM_052813.5(CARD9):c.297G>A (p.Pro99=)	rs115131813	0.01931
NM_052813.5(CARD9):c.1357+16C>T	rs61744202	0.01269
NM_052813.5(CARD9):c.870G>A (p.Ala290=)	rs115057256	0.01248
NM_052813.5(CARD9):c.951+9_951+10del	rs754404646	0.00677
NM_052813.5(CARD9):c.809A>T (p.Glu270Val)	rs114895119	0.00356
NM_052813.5(CARD9):c.1596C>T (p.Asp532=)	rs151057624	0.00191
NM_052813.5(CARD9):c.324C>T (p.Asp108=)	rs34971035	0.00147
NM_052813.5(CARD9):c.1311+18C>T	rs200873988	0.00125
NM_052813.5(CARD9):c.24C>T (p.Asp8=)	rs148523221	0.00109
NM_052813.5(CARD9):c.288C>A (p.Gly96=)	rs137986801	0.00096
NM_052813.5(CARD9):c.627+4C>T	rs181987989	0.00080
NM_052813.5(CARD9):c.951+14C>T	rs574158361	0.00075
NM_052813.5(CARD9):c.1551G>A (p.Gln517=)	rs77469895	0.00067
NM_052813.5(CARD9):c.808-11G>T	rs528166226	0.00048
NM_052813.5(CARD9):c.513C>T (p.Gly171=)	rs78538457	0.00028
NM_052813.5(CARD9):c.661G>A (p.Glu221Lys)	rs200735402	0.00006
NM_052813.5(CARD9):c.808-8C>T	rs542391727	0.00004
NM_052813.5(CARD9):c.1153G>C (p.Val385Leu)	rs3124993
NM_052813.5(CARD9):c.1383G>A (p.Pro461=)	rs138344913
NM_052813.5(CARD9):c.1434+13del
NM_052813.5(CARD9):c.1511+17del	rs2538651536
NM_052813.5(CARD9):c.627+17dup	rs769711471
NM_052813.5(CARD9):c.808-9C>A	rs200458322

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