ClinVar Miner

List of variants in gene IL1RN 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: 65
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HGVS dbSNP gnomAD frequency
NM_173842.3(IL1RN):c.*310T>C rs4252027 0.01657
NM_173842.3(IL1RN):c.459C>T (p.Asp153=) rs4252023 0.01650
NM_173841.2(IL1RN):c.-83G>A rs45526933 0.00580
NM_173842.3(IL1RN):c.69G>A (p.Thr23=) rs2232353 0.00055
NM_173842.3(IL1RN):c.117-9C>T rs373136455 0.00021
NM_173841.2(IL1RN):c.*1156T>C rs140343304 0.00015
NM_173842.3(IL1RN):c.529G>A (p.Glu177Lys) rs114929884 0.00011
NM_173842.3(IL1RN):c.116+15A>G rs138621002 0.00006
NM_173842.3(IL1RN):c.447G>A (p.Ala149=) rs111516567 0.00005
NM_173842.3(IL1RN):c.*1039C>T rs559281814 0.00004
NM_173842.3(IL1RN):c.206-11T>C rs372847811 0.00004
NM_173842.3(IL1RN):c.318+17G>A rs373621697 0.00004
NM_173842.3(IL1RN):c.495C>T (p.Gly165=) rs368843442 0.00004
NM_173842.3(IL1RN):c.414T>C (p.Ser138=) rs146491054 0.00003
NM_173842.3(IL1RN):c.489C>T (p.Asp163=) rs371472986 0.00003
NM_173842.3(IL1RN):c.219G>A (p.Val73=) rs767496834 0.00002
NM_173842.3(IL1RN):c.261A>G (p.Gly87=) rs770774243 0.00002
NM_173842.3(IL1RN):c.486T>C (p.Pro162=) rs772299998 0.00002
NM_173841.3(IL1RN):c.11-16A>C rs747837384 0.00001
NM_173841.3(IL1RN):c.66C>T (p.Asp22=) rs760885026 0.00001
NM_173841.3(IL1RN):c.73+10T>C rs745408148 0.00001
NM_173842.3(IL1RN):c.108A>G (p.Gln36=) rs144691672 0.00001
NM_173842.3(IL1RN):c.156C>T (p.Asn52=) rs1022748861 0.00001
NM_173842.3(IL1RN):c.186A>G (p.Gly62=) rs545976021 0.00001
NM_173842.3(IL1RN):c.192T>C (p.Asn64=) rs146473306 0.00001
NM_173842.3(IL1RN):c.206-4C>G rs759542463 0.00001
NM_173842.3(IL1RN):c.336C>T (p.Asp112=) rs751937390 0.00001
NM_173842.3(IL1RN):c.342C>T (p.Ser114=) rs368859169 0.00001
NM_173842.3(IL1RN):c.366C>T (p.Arg122=) rs139208403 0.00001
NM_173842.3(IL1RN):c.417C>T (p.Ala139=) rs55640833 0.00001
NM_173842.3(IL1RN):c.426C>T (p.Pro142=) rs761311365 0.00001
NM_173842.3(IL1RN):c.528C>T (p.Asp176=) rs192597507 0.00001
NM_173841.3(IL1RN):c.10+11T>C
NM_173841.3(IL1RN):c.10+14A>C
NM_173841.3(IL1RN):c.10+18dup
NM_173841.3(IL1RN):c.11-17C>T
NM_173841.3(IL1RN):c.48A>G (p.Glu16=) rs2104437489
NM_173841.3(IL1RN):c.73+18T>C
NM_173842.3(IL1RN):c.111C>T (p.Ala37=)
NM_173842.3(IL1RN):c.114C>T (p.Phe38=)
NM_173842.3(IL1RN):c.116+10C>A
NM_173842.3(IL1RN):c.116+13C>T
NM_173842.3(IL1RN):c.117-17G>C
NM_173842.3(IL1RN):c.117-18A>C
NM_173842.3(IL1RN):c.141C>G (p.Thr47=) rs2104455713
NM_173842.3(IL1RN):c.159C>T (p.Asn53=)
NM_173842.3(IL1RN):c.205+15G>A
NM_173842.3(IL1RN):c.207A>G (p.Glu69=) rs1274769729
NM_173842.3(IL1RN):c.243G>A (p.Leu81=) rs1457547311
NM_173842.3(IL1RN):c.258T>C (p.His86=)
NM_173842.3(IL1RN):c.274C>T (p.Leu92=)
NM_173842.3(IL1RN):c.300G>A (p.Glu100=) rs776628808
NM_173842.3(IL1RN):c.315G>A (p.Leu105=)
NM_173842.3(IL1RN):c.319-12T>C
NM_173842.3(IL1RN):c.319-16_319-12del rs2104462201
NM_173842.3(IL1RN):c.319-20G>T
NM_173842.3(IL1RN):c.337C>T (p.Leu113=)
NM_173842.3(IL1RN):c.369C>T (p.Phe123=)
NM_173842.3(IL1RN):c.384A>T (p.Ser128=) rs202172114
NM_173842.3(IL1RN):c.396C>G (p.Pro132=)
NM_173842.3(IL1RN):c.426C>G (p.Pro142=) rs761311365
NM_173842.3(IL1RN):c.444A>G (p.Thr148=)
NM_173842.3(IL1RN):c.519C>T (p.Phe173=)
NM_173842.3(IL1RN):c.534G>A (p.Ter178=)
NM_173842.3(IL1RN):c.57C>G (p.Phe19Leu)

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