ClinVar Miner

List of variants in gene IL21R 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: 120
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HGVS dbSNP gnomAD frequency
NM_181078.3(IL21R):c.137C>T (p.Thr46Met) rs137946070 0.00360
NM_181078.3(IL21R):c.571C>T (p.Arg191Cys) rs3093370 0.00069
NM_181078.3(IL21R):c.19G>A (p.Ala7Thr) rs145338579 0.00058
NM_181078.3(IL21R):c.426C>T (p.Tyr142=) rs137868301 0.00054
NM_181078.3(IL21R):c.415C>T (p.Arg139Cys) rs146177564 0.00053
NM_181078.3(IL21R):c.786-14C>G rs202012016 0.00039
NM_181078.3(IL21R):c.1113C>T (p.Tyr371=) rs145529117 0.00030
NM_181078.3(IL21R):c.352+16C>T rs368431181 0.00027
NM_181078.3(IL21R):c.582G>A (p.Ser194=) rs142037270 0.00027
NM_181078.3(IL21R):c.81C>T (p.Thr27=) rs373735352 0.00021
NM_181078.3(IL21R):c.402T>C (p.Tyr134=) rs56189419 0.00011
NM_181078.3(IL21R):c.270C>T (p.Ala90=) rs201431824 0.00010
NM_181078.3(IL21R):c.786-16C>T rs56168417 0.00010
NM_181078.3(IL21R):c.50-16C>T rs369236227 0.00009
NM_181078.3(IL21R):c.63C>T (p.Pro21=) rs147702809 0.00006
NM_181078.3(IL21R):c.1059G>A (p.Pro353=) rs374745479 0.00005
NM_181078.3(IL21R):c.252T>C (p.Asp84=) rs1183434798 0.00005
NM_181078.3(IL21R):c.339C>T (p.Leu113=) rs201430379 0.00004
NM_181078.3(IL21R):c.660G>A (p.Pro220=) rs747035204 0.00004
NM_181078.3(IL21R):c.96G>A (p.Thr32=) rs187217568 0.00004
NM_181078.3(IL21R):c.357G>A (p.Lys119=) rs777661467 0.00003
NM_181078.3(IL21R):c.855C>T (p.Ser285=) rs374663077 0.00003
NM_181078.3(IL21R):c.867+9C>T rs1401561548 0.00003
NM_181078.3(IL21R):c.1191C>T (p.Asp397=) rs750369453 0.00002
NM_181078.3(IL21R):c.152+10C>T rs761690967 0.00002
NM_181078.3(IL21R):c.786-9C>A rs756596754 0.00002
NM_181078.3(IL21R):c.867+11G>A rs763080402 0.00002
NM_181078.3(IL21R):c.1266G>C (p.Gly422=) rs760423765 0.00001
NM_181078.3(IL21R):c.1275C>G (p.Val425=) rs763777534 0.00001
NM_181078.3(IL21R):c.138G>A (p.Thr46=) rs771721185 0.00001
NM_181078.3(IL21R):c.152+11G>A rs769726854 0.00001
NM_181078.3(IL21R):c.153-20C>T rs3093401 0.00001
NM_181078.3(IL21R):c.1593G>A (p.Ser531=) rs926286373 0.00001
NM_181078.3(IL21R):c.18C>T (p.Ala6=) rs559479535 0.00001
NM_181078.3(IL21R):c.213C>T (p.Ala71=) rs529309087 0.00001
NM_181078.3(IL21R):c.24C>T (p.Pro8=) rs777584572 0.00001
NM_181078.3(IL21R):c.273C>T (p.Asp91=) rs761924013 0.00001
NM_181078.3(IL21R):c.348G>A (p.Glu116=) rs752444834 0.00001
NM_181078.3(IL21R):c.353-9T>C rs1294727591 0.00001
NM_181078.3(IL21R):c.381T>C (p.Thr127=) rs1261615952 0.00001
NM_181078.3(IL21R):c.39G>A (p.Leu13=) rs780077018 0.00001
NM_181078.3(IL21R):c.513G>A (p.Pro171=) rs752443447 0.00001
NM_181078.3(IL21R):c.516G>A (p.Arg172=) rs1485014350 0.00001
NM_181078.3(IL21R):c.555C>T (p.Leu185=) rs2087444518 0.00001
NM_181078.3(IL21R):c.609G>A (p.Gly203=) rs755926054 0.00001
NM_181078.3(IL21R):c.69C>T (p.Leu23=) rs202066831 0.00001
NM_181078.3(IL21R):c.723C>T (p.Leu241=) rs1240842516 0.00001
NM_181078.3(IL21R):c.753C>T (p.Ala251=) rs1237106214 0.00001
NM_181078.3(IL21R):c.785+10G>C rs1185644382 0.00001
NM_181078.3(IL21R):c.785+19G>T rs778601431 0.00001
NM_181078.3(IL21R):c.807C>T (p.Ala269=) rs746467550 0.00001
NM_181078.3(IL21R):c.909G>A (p.Leu303=) rs995647199 0.00001
NM_181078.3(IL21R):c.942G>A (p.Leu314=) rs758862352 0.00001
NM_181078.3(IL21R):c.975G>A (p.Pro325=) rs543436759 0.00001
NM_181078.3(IL21R):c.1074G>A (p.Ser358=)
NM_181078.3(IL21R):c.1080C>T (p.Gly360=)
NM_181078.3(IL21R):c.1107G>A (p.Arg369=)
NM_181078.3(IL21R):c.1143G>C (p.Val381=) rs752449999
NM_181078.3(IL21R):c.1155G>A (p.Glu385=)
NM_181078.3(IL21R):c.1173C>T (p.Pro391=)
NM_181078.3(IL21R):c.1212G>A (p.Leu404=)
NM_181078.3(IL21R):c.1236A>C (p.Pro412=) rs772608088
NM_181078.3(IL21R):c.1236A>T (p.Pro412=) rs772608088
NM_181078.3(IL21R):c.126C>T (p.Leu42=) rs777897180
NM_181078.3(IL21R):c.1326G>A (p.Leu442=)
NM_181078.3(IL21R):c.141C>A (p.Leu47=)
NM_181078.3(IL21R):c.144C>T (p.Thr48=) rs2141290474
NM_181078.3(IL21R):c.152+10C>A rs761690967
NM_181078.3(IL21R):c.152+11G>C rs769726854
NM_181078.3(IL21R):c.152+18_152+19del
NM_181078.3(IL21R):c.152+20C>G
NM_181078.3(IL21R):c.152+7_152+23del rs768314938
NM_181078.3(IL21R):c.1581T>C (p.Pro527=)
NM_181078.3(IL21R):c.1584G>C (p.Pro528=) rs370397954
NM_181078.3(IL21R):c.1590T>G (p.Leu530=)
NM_181078.3(IL21R):c.1602A>T (p.Gly534=)
NM_181078.3(IL21R):c.1605C>G (p.Pro535=)
NM_181078.3(IL21R):c.180C>T (p.Asp60=)
NM_181078.3(IL21R):c.205A>C (p.Arg69=)
NM_181078.3(IL21R):c.210G>A (p.Ser70=)
NM_181078.3(IL21R):c.225G>A (p.Thr75=)
NM_181078.3(IL21R):c.246C>T (p.His82=)
NM_181078.3(IL21R):c.352+18C>T
NM_181078.3(IL21R):c.352+20A>C
NM_181078.3(IL21R):c.352+9C>G
NM_181078.3(IL21R):c.353-18C>T
NM_181078.3(IL21R):c.353-4C>A
NM_181078.3(IL21R):c.375C>T (p.Asn125=)
NM_181078.3(IL21R):c.465G>A (p.Gln155=)
NM_181078.3(IL21R):c.49+15C>T
NM_181078.3(IL21R):c.49+16G>A
NM_181078.3(IL21R):c.50-18T>C
NM_181078.3(IL21R):c.50-4C>T
NM_181078.3(IL21R):c.508-30_508-20del rs2087443169
NM_181078.3(IL21R):c.558C>T (p.Leu186=)
NM_181078.3(IL21R):c.561C>G (p.Pro187=)
NM_181078.3(IL21R):c.561C>T (p.Pro187=)
NM_181078.3(IL21R):c.685+15G>A
NM_181078.3(IL21R):c.686-17C>A
NM_181078.3(IL21R):c.688T>C (p.Leu230=)
NM_181078.3(IL21R):c.714G>A (p.Leu238=)
NM_181078.3(IL21R):c.72C>T (p.Val24=) rs1596586040
NM_181078.3(IL21R):c.741C>G (p.Val247=)
NM_181078.3(IL21R):c.756C>T (p.Phe252=)
NM_181078.3(IL21R):c.785+19G>A
NM_181078.3(IL21R):c.786-18C>T
NM_181078.3(IL21R):c.786-25_786-19del
NM_181078.3(IL21R):c.786-5C>A
NM_181078.3(IL21R):c.786-5C>T rs779223620
NM_181078.3(IL21R):c.786-6C>G
NM_181078.3(IL21R):c.786-8C>T
NM_181078.3(IL21R):c.798G>A (p.Lys266=)
NM_181078.3(IL21R):c.867+10C>T
NM_181078.3(IL21R):c.867+16T>C
NM_181078.3(IL21R):c.903G>T (p.Leu301=)
NM_181078.3(IL21R):c.90C>T (p.Leu30=) rs1596586066
NM_181078.3(IL21R):c.933C>T (p.Pro311=)
NM_181078.3(IL21R):c.96G>C (p.Thr32=) rs187217568
NM_181078.3(IL21R):c.978C>A (p.Ala326=)
NM_181078.3(IL21R):c.978C>G (p.Ala326=) rs2087528777

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