ClinVar Miner

List of variants reported as likely benign for Inflammatory bowel disease

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_002273.4(KRT8):c.187A>G (p.Ile63Val) rs59536457 0.00302
NM_000572.3(IL10):c.345C>T (p.Asn115=) rs5743626 0.00073
NM_000572.3(IL10):c.56G>A (p.Ser19Asn) rs139073251 0.00056
NM_000572.3(IL10):c.225+18G>A rs376490444 0.00033
NM_000572.3(IL10):c.165+15T>C rs373813224 0.00006
NM_000572.3(IL10):c.228T>C (p.Gly76=) rs139352858 0.00004
NM_000572.3(IL10):c.309A>G (p.Pro103=) rs987614203 0.00004
NM_000572.3(IL10):c.30G>C (p.Leu10=) rs762421652 0.00004
NM_000572.3(IL10):c.379-19T>G rs759391400 0.00004
NM_000572.3(IL10):c.321G>A (p.Ala107=) rs560908141 0.00003
NM_000572.3(IL10):c.225+15G>A rs1342823726 0.00002
NM_000572.3(IL10):c.165+20G>A rs749899175 0.00001
NM_000572.3(IL10):c.18G>A (p.Leu6=) rs760242157 0.00001
NM_000572.3(IL10):c.225+17G>A rs1674832645 0.00001
NM_000572.3(IL10):c.255G>A (p.Glu85=) rs769682299 0.00001
NM_000572.3(IL10):c.297G>A (p.Glu99=) rs1220388430 0.00001
NM_000572.3(IL10):c.336G>C (p.Leu112=) rs767727378 0.00001
NM_000572.3(IL10):c.393C>T (p.Pro131=) rs1229974502 0.00001
NM_000572.3(IL10):c.48G>A (p.Val16=) rs780213087 0.00001
NM_000572.3(IL10):c.6C>T (p.His2=) rs140486772 0.00001
NM_000572.3(IL10):c.135A>C (p.Arg45=)
NM_000572.3(IL10):c.165+14C>T
NM_000572.3(IL10):c.166-19C>T
NM_000572.3(IL10):c.166-7C>T
NM_000572.3(IL10):c.201G>A (p.Lys67=) rs2102439750
NM_000572.3(IL10):c.213G>T (p.Leu71=)
NM_000572.3(IL10):c.225+20G>A
NM_000572.3(IL10):c.252T>G (p.Ser84=)
NM_000572.3(IL10):c.261C>T (p.Ile87=)
NM_000572.3(IL10):c.273G>A (p.Leu91=) rs1674815134
NM_000572.3(IL10):c.276G>A (p.Glu92=) rs1674814817
NM_000572.3(IL10):c.327G>A (p.Val109=)
NM_000572.3(IL10):c.334C>T (p.Leu112=) rs2102439153
NM_000572.3(IL10):c.361C>T (p.Leu121=)
NM_000572.3(IL10):c.372G>A (p.Arg124=)
NM_000572.3(IL10):c.375C>A (p.Arg125=) rs755403362
NM_000572.3(IL10):c.378+15A>C
NM_000572.3(IL10):c.378+16G>C
NM_000572.3(IL10):c.378+19_378+20delinsCC rs2102439038
NM_000572.3(IL10):c.379-16C>T
NM_000572.3(IL10):c.379-17T>C
NM_000572.3(IL10):c.414C>G (p.Ala138=)
NM_000572.3(IL10):c.444+17G>A
NM_000572.3(IL10):c.444+20G>A
NM_000572.3(IL10):c.444+8T>C
NM_000572.3(IL10):c.445-8C>T
NM_000572.3(IL10):c.471C>A (p.Ala157=) rs1674735790
NM_000572.3(IL10):c.471C>T (p.Ala157=)
NM_000572.3(IL10):c.510C>T (p.Ala170=) rs142093260
NM_000572.3(IL10):c.513C>T (p.Tyr171=) rs1572537757
NM_000572.3(IL10):c.84C>T (p.Asn28=) rs945097885
NM_001558.4(IL10RA):c.*356dup rs146951811

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