ClinVar Miner

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

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_001366385.1(CARD14):c.2267G>A (p.Cys756Tyr) rs34822755 0.01019
NM_001366385.1(CARD14):c.1917C>T (p.Ala639=) rs79407194 0.00344
NM_001366385.1(CARD14):c.2139C>T (p.Cys713=) rs142449734 0.00025
NM_001366385.1(CARD14):c.2190C>T (p.Ala730=) rs146968151 0.00025
NM_001366385.1(CARD14):c.2094T>C (p.His698=) rs145420791 0.00010
NM_001366385.1(CARD14):c.2784C>T (p.Asn928=) rs140536892 0.00007
NM_001366385.1(CARD14):c.1923G>C (p.Gly641=) rs931477418 0.00006
NM_001366385.1(CARD14):c.1977C>T (p.Asp659=) rs200737962 0.00006
NM_001366385.1(CARD14):c.1978+20C>T rs370551701 0.00006
NM_001366385.1(CARD14):c.2112C>T (p.His704=) rs751083330 0.00006
NM_001366385.1(CARD14):c.1852-14C>T rs377407058 0.00005
NM_001366385.1(CARD14):c.1860C>T (p.Tyr620=) rs148265488 0.00005
NM_001366385.1(CARD14):c.1962G>A (p.Val654=) rs747461948 0.00004
NM_001366385.1(CARD14):c.2219+13C>T rs759246881 0.00004
NM_001366385.1(CARD14):c.2284-20T>C rs774816663 0.00004
NM_001366385.1(CARD14):c.2889G>A (p.Ala963=) rs761925557 0.00004
NM_001366385.1(CARD14):c.2808-19_2808-18insA rs763555855 0.00003
NM_001366385.1(CARD14):c.2219+16G>A rs762319448 0.00002
NM_001366385.1(CARD14):c.2307G>A (p.Lys769=) rs778848984 0.00002
NM_001366385.1(CARD14):c.2692-17C>T rs1373202027 0.00002
NM_001366385.1(CARD14):c.1902G>A (p.Thr634=) rs1003951860 0.00001
NM_001366385.1(CARD14):c.1938G>A (p.Val646=) rs1255773294 0.00001
NM_001366385.1(CARD14):c.1941C>T (p.Asp647=) rs777602482 0.00001
NM_001366385.1(CARD14):c.1974G>A (p.Thr658=) rs776920670 0.00001
NM_001366385.1(CARD14):c.2019G>A (p.Ala673=) rs1024202736 0.00001
NM_001366385.1(CARD14):c.2025G>A (p.Ser675=) rs778055809 0.00001
NM_001366385.1(CARD14):c.2064G>A (p.Glu688=) rs1598696214 0.00001
NM_001366385.1(CARD14):c.2118C>T (p.Thr706=) rs539561719 0.00001
NM_001366385.1(CARD14):c.2160C>T (p.Arg720=) rs776598351 0.00001
NM_001366385.1(CARD14):c.2196C>T (p.His732=) rs758642695 0.00001
NM_001366385.1(CARD14):c.2274G>A (p.Val758=) rs777889815 0.00001
NM_001366385.1(CARD14):c.2284-11C>T rs767976234 0.00001
NM_001366385.1(CARD14):c.2352G>A (p.Leu784=) rs1037309214 0.00001
NM_001366385.1(CARD14):c.2692-19T>C rs1292977579 0.00001
NM_001366385.1(CARD14):c.2694C>T (p.Asn898=) rs1045266295 0.00001
NM_001366385.1(CARD14):c.2808-18C>G rs910909016 0.00001
NM_001366385.1(CARD14):c.2841G>A (p.Glu947=) rs201650186 0.00001
NM_001366385.1(CARD14):c.2937C>T (p.Asp979=) rs957038309 0.00001
NM_001366385.1(CARD14):c.2973C>T (p.Asp991=) rs554956821 0.00001
NM_001366385.1(CARD14):c.1852-11C>T
NM_001366385.1(CARD14):c.1852-18T>C
NM_001366385.1(CARD14):c.1852-7C>T rs2040987039
NM_001366385.1(CARD14):c.1854T>G (p.Val618=) rs111451894
NM_001366385.1(CARD14):c.1869A>G (p.Ser623=)
NM_001366385.1(CARD14):c.1920G>A (p.Val640=)
NM_001366385.1(CARD14):c.1929C>G (p.Leu643=) rs2144430849
NM_001366385.1(CARD14):c.1938G>T (p.Val646=) rs1255773294
NM_001366385.1(CARD14):c.1971C>T (p.Asn657=) rs2144433219
NM_001366385.1(CARD14):c.1978+12A>C
NM_001366385.1(CARD14):c.1978+15C>A rs774496431
NM_001366385.1(CARD14):c.1978+17T>C rs1198880344
NM_001366385.1(CARD14):c.1979-10C>T
NM_001366385.1(CARD14):c.1979-13C>A rs377635873
NM_001366385.1(CARD14):c.1986G>A (p.Lys662=) rs1425514742
NM_001366385.1(CARD14):c.1990C>T (p.Leu664=)
NM_001366385.1(CARD14):c.2010C>G (p.Ala670=)
NM_001366385.1(CARD14):c.2019G>T (p.Ala673=)
NM_001366385.1(CARD14):c.2037C>T (p.Phe679=)
NM_001366385.1(CARD14):c.2058C>T (p.Ala686=)
NM_001366385.1(CARD14):c.2100C>T (p.Asn700=)
NM_001366385.1(CARD14):c.2115C>T (p.Val705=)
NM_001366385.1(CARD14):c.2151T>C (p.His717=)
NM_001366385.1(CARD14):c.2163G>A (p.Val721=)
NM_001366385.1(CARD14):c.2172C>T (p.Tyr724=)
NM_001366385.1(CARD14):c.2219+15C>T
NM_001366385.1(CARD14):c.2220-13C>A
NM_001366385.1(CARD14):c.2220-19C>A
NM_001366385.1(CARD14):c.2244C>T (p.Leu748=)
NM_001366385.1(CARD14):c.2271C>T (p.Thr757=)
NM_001366385.1(CARD14):c.2283+14G>A
NM_001366385.1(CARD14):c.2284-15C>T
NM_001366385.1(CARD14):c.2292T>C (p.Ser764=)
NM_001366385.1(CARD14):c.2310G>A (p.Leu770=) rs750412113
NM_001366385.1(CARD14):c.2319C>T (p.Ile773=) rs747692472
NM_001366385.1(CARD14):c.2322C>T (p.Val774=) rs1598706887
NM_001366385.1(CARD14):c.2692-5C>A rs777494484
NM_001366385.1(CARD14):c.2692-8C>A rs756059561
NM_001366385.1(CARD14):c.2769C>T (p.Ile923=)
NM_001366385.1(CARD14):c.2807+10C>G rs368700533
NM_001366385.1(CARD14):c.2807+8C>A
NM_001366385.1(CARD14):c.2808-15C>A rs549404117
NM_001366385.1(CARD14):c.2808-15C>T rs549404117
NM_001366385.1(CARD14):c.2808-19C>T
NM_001366385.1(CARD14):c.2808-20C>G rs545159633
NM_001366385.1(CARD14):c.2808-20C>T
NM_001366385.1(CARD14):c.2808-20_2808-19delinsAA rs2144635630
NM_001366385.1(CARD14):c.2848C>T (p.Leu950=)
NM_001366385.1(CARD14):c.2871G>A (p.Glu957=) rs373510767
NM_001366385.1(CARD14):c.2877C>T (p.Asp959=)
NM_001366385.1(CARD14):c.2919C>T (p.Asp973=) rs144285237
NM_001366385.1(CARD14):c.2946C>A (p.Leu982=)
NM_001366385.1(CARD14):c.2949C>T (p.Ser983=) rs747407619
NM_001366385.1(CARD14):c.2958C>T (p.Arg986=)
NM_001366385.1(CARD14):c.2967C>T (p.Ile989=)
NM_001366385.1(CARD14):c.2970C>A (p.Ala990=) rs376031523
NM_001366385.1(CARD14):c.2970C>T (p.Ala990=) rs376031523
NM_001366385.1(CARD14):c.2997G>C (p.Thr999=) rs1411024608

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