ClinVar Miner

List of variants in gene IL10, IL19, LOC128462409 studied for Inflammatory bowel disease

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000572.3(IL10):c.43G>A (p.Gly15Arg) rs145922845 0.00186
NM_000572.3(IL10):c.56G>A (p.Ser19Asn) rs139073251 0.00056
NM_000572.3(IL10):c.58C>T (p.Pro20Ser) rs141219090 0.00038
NM_000572.3(IL10):c.165+15T>C rs373813224 0.00006
NM_000572.3(IL10):c.30G>C (p.Leu10=) rs762421652 0.00004
NM_000572.3(IL10):c.134G>A (p.Arg45Gln) rs550164520 0.00002
NM_000572.3(IL10):c.37C>A (p.Leu13Met) rs769236514 0.00002
NM_000572.3(IL10):c.121C>T (p.Leu41Phe) rs750010814 0.00001
NM_000572.3(IL10):c.165+20G>A rs749899175 0.00001
NM_000572.3(IL10):c.165+8T>C rs530302888 0.00001
NM_000572.3(IL10):c.18G>A (p.Leu6=) rs760242157 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.100C>A (p.Pro34Thr) rs2102441015
NM_000572.3(IL10):c.112C>G (p.Pro38Ala)
NM_000572.3(IL10):c.118A>G (p.Met40Val)
NM_000572.3(IL10):c.135A>C (p.Arg45=)
NM_000572.3(IL10):c.137A>G (p.Asp46Gly)
NM_000572.3(IL10):c.165+14C>T
NM_000572.3(IL10):c.46G>T (p.Val16Leu) rs1674878129
NM_000572.3(IL10):c.62G>A (p.Gly21Asp)
NM_000572.3(IL10):c.71C>G (p.Thr24Ser) rs1674877288
NM_000572.3(IL10):c.84C>T (p.Asn28=) rs945097885
NM_000572.3(IL10):c.92C>T (p.Thr31Ile)
NM_000572.3(IL10):c.94C>A (p.His32Asn) rs376787667

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