List of variants in gene combination CARD14, SGSH reported as benign for immune system disorder

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.1852-60T>C	rs2304856	0.51286
NM_001366385.1(CARD14):c.2398+42T>C	rs4889836	0.41735
NM_001366385.1(CARD14):c.2398+30A>G	rs4889996	0.41701
NM_001366385.1(CARD14):c.2398+49G>A	rs4889997	0.40159
NM_001366385.1(CARD14):c.1979-125C>A	rs3813063	0.39784
NM_001366385.1(CARD14):c.2283+11A>C	rs9905662	0.07362
NM_001366385.1(CARD14):c.2885G>A (p.Arg962Gln)	rs34850974	0.04584
NM_001366385.1(CARD14):c.2853G>A (p.Glu951=)	rs78569961	0.01590
NM_001366385.1(CARD14):c.2044C>T (p.Arg682Trp)	rs117918077	0.01097
NM_001366385.1(CARD14):c.2267G>A (p.Cys756Tyr)	rs34822755	0.01019
NM_001366385.1(CARD14):c.2193G>A (p.Ala731=)	rs35692270	0.00788
NM_001366385.1(CARD14):c.2772C>T (p.His924=)	rs146356100	0.00593
NM_001366385.1(CARD14):c.2763C>T (p.Ile921=)	rs150378107	0.00572
NM_001366385.1(CARD14):c.2829C>T (p.Gly943=)	rs200640336	0.00496
NM_001366385.1(CARD14):c.2822G>A (p.Arg941Gln)	rs74000616	0.00421
NM_001366385.1(CARD14):c.2859G>A (p.Ala953=)	rs139969019	0.00386
NM_001366385.1(CARD14):c.1917C>T (p.Ala639=)	rs79407194	0.00344
NM_001366385.1(CARD14):c.1979-15G>A	rs199898989	0.00303
NM_001366385.1(CARD14):c.2335G>A (p.Ala779Thr)	rs141913003	0.00220
NM_001366385.1(CARD14):c.1852-16C>T	rs186883652	0.00139
NM_001366385.1(CARD14):c.2140G>A (p.Gly714Ser)	rs151150961	0.00035
NM_001366385.1(CARD14):c.1852-8G>A	rs544120287	0.00023
NM_001366385.1(CARD14):c.2807+10C>T	rs368700533	0.00019
NM_001366385.1(CARD14):c.2398+14A>C	rs573376427	0.00003
NM_001366385.1(CARD14):c.2775C>T (p.Val925=)	rs372790630	0.00003
NM_001366385.1(CARD14):c.1998G>A (p.Gln666=)	rs142087113	0.00002
NM_001366385.1(CARD14):c.2219+14T>A	rs8069255
NM_001366385.1(CARD14):c.2219+14T>G	rs8069255
NM_001366385.1(CARD14):c.2808-19C>A	rs111745899
NM_001366385.1(CARD14):c.2808-19C>G	rs111745899
NM_001366385.1(CARD14):c.2808-20C>A	rs545159633
NM_001366385.1(CARD14):c.2919C>G (p.Asp973Glu)	rs144285237

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