ClinVar Miner

List of variants in gene IL36RN reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_012275.3(IL36RN):c.*1902T>C rs28939968 0.01844
NM_012275.3(IL36RN):c.*308T>G rs114200724 0.01255
NM_012275.3(IL36RN):c.*1660G>A rs74502334 0.01253
NM_012275.3(IL36RN):c.*1763G>A rs72946729 0.00725
NM_012275.3(IL36RN):c.140A>G (p.Asn47Ser) rs28938777 0.00348
NM_012275.3(IL36RN):c.169G>A (p.Val57Ile) rs77864207 0.00124
NM_012275.3(IL36RN):c.363G>A (p.Leu121=) rs151274071 0.00070
NM_012275.3(IL36RN):c.*281G>A rs80220660 0.00054
NM_012275.3(IL36RN):c.115+15A>G rs200453384 0.00039
NM_012275.3(IL36RN):c.30-12C>T rs764444805 0.00013
NM_012275.3(IL36RN):c.244-6C>T rs374849220 0.00009
NM_012275.3(IL36RN):c.436A>G (p.Ile146Val) rs202059991 0.00007
NM_012275.3(IL36RN):c.245C>T (p.Pro82Leu) rs144182857 0.00006
NM_012275.3(IL36RN):c.447C>T (p.Phe149=) rs201107219 0.00006
NM_012275.3(IL36RN):c.240A>G (p.Leu80=) rs148271084 0.00005
NM_012275.3(IL36RN):c.306G>A (p.Arg102=) rs143557954 0.00004
NM_012275.3(IL36RN):c.351G>A (p.Pro117=) rs202161658 0.00004
NM_012275.3(IL36RN):c.115+7G>A rs760803052 0.00003
NM_012275.3(IL36RN):c.168C>T (p.Pro56=) rs549588385 0.00003
NM_012275.3(IL36RN):c.244-15C>T rs749973247 0.00003
NM_012275.3(IL36RN):c.244-13C>T rs762586699 0.00002
NM_012275.3(IL36RN):c.102G>A (p.Gly34=) rs941319736 0.00001
NM_012275.3(IL36RN):c.228G>A (p.Pro76=) rs774906497 0.00001
NM_012275.3(IL36RN):c.291C>T (p.Ser97=) rs1573387667 0.00001
NM_012275.3(IL36RN):c.333C>T (p.Phe111=) rs199824136 0.00001
NM_012275.3(IL36RN):c.375T>C (p.Pro125=) rs775413713 0.00001
NM_012275.3(IL36RN):c.381C>T (p.Ala127=) rs760489144 0.00001
NM_012275.3(IL36RN):c.411C>T (p.Pro137=) rs765211863 0.00001
NM_012275.3(IL36RN):c.75G>A (p.Gln25=) rs1348538791 0.00001
NM_012275.3(IL36RN):c.115+14C>T
NM_012275.3(IL36RN):c.115+9T>C
NM_012275.3(IL36RN):c.116-11C>T
NM_012275.3(IL36RN):c.116-5C>G rs2105069232
NM_012275.3(IL36RN):c.116-6C>T
NM_012275.3(IL36RN):c.144G>C (p.Arg48=)
NM_012275.3(IL36RN):c.148C>T (p.Leu50=)
NM_012275.3(IL36RN):c.165C>A (p.Ser55=) rs2105069324
NM_012275.3(IL36RN):c.165C>T (p.Ser55=)
NM_012275.3(IL36RN):c.18G>A (p.Ala6=) rs577280688
NM_012275.3(IL36RN):c.210T>C (p.Cys70=)
NM_012275.3(IL36RN):c.243+16T>C rs2105069464
NM_012275.3(IL36RN):c.244-10C>A
NM_012275.3(IL36RN):c.244-13C>A rs762586699
NM_012275.3(IL36RN):c.244-17C>T
NM_012275.3(IL36RN):c.244-9_244-6del rs749941611
NM_012275.3(IL36RN):c.282A>G (p.Glu94=)
NM_012275.3(IL36RN):c.29+15C>A rs1476532102
NM_012275.3(IL36RN):c.29+15C>G rs1476532102
NM_012275.3(IL36RN):c.29+7G>A
NM_012275.3(IL36RN):c.30-13C>T
NM_012275.3(IL36RN):c.30-18C>A
NM_012275.3(IL36RN):c.307C>A (p.Arg103=)
NM_012275.3(IL36RN):c.348C>T (p.Tyr116=) rs1383851199
NM_012275.3(IL36RN):c.366C>T (p.Cys122=)
NM_012275.3(IL36RN):c.369G>A (p.Thr123=) rs28938778
NM_012275.3(IL36RN):c.387G>A (p.Gln129=) rs1685666198
NM_012275.3(IL36RN):c.42G>A (p.Ser14=)
NM_012275.3(IL36RN):c.435C>T (p.Pro145=)
NM_012275.3(IL36RN):c.441A>G (p.Thr147=)

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