ClinVar Miner

List of variants in gene combination CARD14, LOC126862662, SGSH reported as likely benign for psoriasis

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_001366385.1(CARD14):c.2569+4T>C rs146678380 0.00181
NM_001366385.1(CARD14):c.2476C>T (p.Arg826Trp) rs139467141 0.00018
NM_001366385.1(CARD14):c.2421C>T (p.Ala807=) rs770965110 0.00004
NM_001366385.1(CARD14):c.2640C>T (p.Ser880=) rs367654497 0.00004
NM_001366385.1(CARD14):c.2691+14C>T rs372429076 0.00003
NM_001366385.1(CARD14):c.2457G>A (p.Val819=) rs763834649 0.00002
NM_001366385.1(CARD14):c.2526C>T (p.Ser842=) rs755430374 0.00002
NM_001366385.1(CARD14):c.2424G>A (p.Glu808=) rs767351855 0.00001
NM_001366385.1(CARD14):c.2535G>A (p.Leu845=) rs1193362044 0.00001
NM_001366385.1(CARD14):c.2544C>T (p.Leu848=) rs1171320109 0.00001
NM_001366385.1(CARD14):c.2570-4G>A rs746900548 0.00001
NM_001366385.1(CARD14):c.2619C>T (p.Ile873=) rs1350847074 0.00001
NM_001366385.1(CARD14):c.2399-6C>T
NM_001366385.1(CARD14):c.2409G>T (p.Thr803=)
NM_001366385.1(CARD14):c.2421C>G (p.Ala807=) rs770965110
NM_001366385.1(CARD14):c.2437C>T (p.Leu813=)
NM_001366385.1(CARD14):c.2463C>T (p.Pro821=)
NM_001366385.1(CARD14):c.2472C>T (p.Pro824=)
NM_001366385.1(CARD14):c.2514G>A (p.Gly838=) rs1452524384
NM_001366385.1(CARD14):c.2544C>G (p.Leu848=)
NM_001366385.1(CARD14):c.2559G>A (p.Lys853=) rs757431534
NM_001366385.1(CARD14):c.2569+10T>G
NM_001366385.1(CARD14):c.2569+13C>G
NM_001366385.1(CARD14):c.2569+8G>A rs373649706
NM_001366385.1(CARD14):c.2570-11G>A
NM_001366385.1(CARD14):c.2570-18G>A
NM_001366385.1(CARD14):c.2570-9C>G rs780352594
NM_001366385.1(CARD14):c.2574C>T (p.Tyr858=)
NM_001366385.1(CARD14):c.2595G>A (p.Glu865=)
NM_001366385.1(CARD14):c.2598C>G (p.Ala866=)
NM_001366385.1(CARD14):c.2628G>A (p.Glu876=)
NM_001366385.1(CARD14):c.2658G>T (p.Val886=)
NM_001366385.1(CARD14):c.2691+10A>T rs1598715259
NM_001366385.1(CARD14):c.2691+11G>A
NM_001366385.1(CARD14):c.2691+16G>T
NM_001366385.1(CARD14):c.2691+19T>G
NM_001366385.1(CARD14):c.2691+20G>A rs2041261946

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