ClinVar Miner

List of variants in gene IL11RA studied for bone disorder

Included ClinVar conditions (1350):
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Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_001142784.3(IL11RA):c.343C>T (p.Arg115Cys) rs200580340 0.00046
NM_001142784.3(IL11RA):c.886C>T (p.Arg296Trp) rs387906784 0.00013
NM_001142784.3(IL11RA):c.475C>T (p.Gln159Ter) rs387906787 0.00006
NM_001142784.3(IL11RA):c.781C>T (p.Arg261Cys) rs201638429 0.00005
NM_001142784.3(IL11RA):c.810G>A (p.Thr270=) rs1258408605 0.00003
NM_001142784.3(IL11RA):c.281G>T (p.Cys94Phe) rs369630361 0.00002
NM_001142784.3(IL11RA):c.662C>G (p.Pro221Arg) rs387906785 0.00001
NM_001142784.3(IL11RA):c.331+2T>C rs1554710108
NM_001142784.3(IL11RA):c.734C>G (p.Ser245Cys) rs387906786
NM_001142784.3(IL11RA):c.907ACCTGGAGC[3] (p.Ser308_Pro309insThrTrpSer)
NM_001142784.3(IL11RA):c.919T>C (p.Trp307Arg)

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