ClinVar Miner

List of variants in gene IL17RC, LOC129936144 studied for immune system disorder

Included ClinVar conditions (908):
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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_153460.4(IL17RC):c.2025G>A (p.Gly675=) rs189013166 0.00194
NM_153460.4(IL17RC):c.2022C>T (p.Ser674=) rs757894385 0.00008
NM_153460.4(IL17RC):c.2152G>A (p.Asp718Asn) rs755919625 0.00008
NM_153460.4(IL17RC):c.2119G>A (p.Gly707Arg) rs576002780 0.00006
NM_153460.4(IL17RC):c.2062C>A (p.Leu688Ile) rs199772854 0.00005
NM_153460.4(IL17RC):c.2137G>A (p.Gly713Arg) rs781031468 0.00004
NM_153460.4(IL17RC):c.2144G>A (p.Gly715Glu) rs752392891 0.00004
NM_153460.4(IL17RC):c.2066A>C (p.Gln689Pro) rs753085510 0.00001
NM_153460.4(IL17RC):c.2125G>C (p.Gly709Arg) rs754096924 0.00001
NM_153460.4(IL17RC):c.2023G>A (p.Gly675Arg)
NM_153460.4(IL17RC):c.2024G>A (p.Gly675Glu)
NM_153460.4(IL17RC):c.2027G>T (p.Arg676Leu)
NM_153460.4(IL17RC):c.2028G>A (p.Arg676=) rs2125321875
NM_153460.4(IL17RC):c.2033A>G (p.Gln678Arg)
NM_153460.4(IL17RC):c.2037G>C (p.Glu679Asp) rs2084997441
NM_153460.4(IL17RC):c.2041G>A (p.Ala681Thr) rs747911271
NM_153460.4(IL17RC):c.2042C>A (p.Ala681Glu) rs371918201
NM_153460.4(IL17RC):c.2042C>T (p.Ala681Val) rs371918201
NM_153460.4(IL17RC):c.2043G>A (p.Ala681=)
NM_153460.4(IL17RC):c.2045A>C (p.Glu682Ala) rs988221789
NM_153460.4(IL17RC):c.2046G>T (p.Glu682Asp)
NM_153460.4(IL17RC):c.2047C>T (p.Gln683Ter) rs2084999838
NM_153460.4(IL17RC):c.2057G>A (p.Arg686Gln)
NM_153460.4(IL17RC):c.2059G>A (p.Ala687Thr) rs572542208
NM_153460.4(IL17RC):c.2065C>T (p.Gln689Ter) rs2125322571
NM_153460.4(IL17RC):c.2067G>A (p.Gln689=) rs2125322609
NM_153460.4(IL17RC):c.2071G>T (p.Ala691Ser)
NM_153460.4(IL17RC):c.2076G>A (p.Leu692=)
NM_153460.4(IL17RC):c.2084A>C (p.Tyr695Ser)
NM_153460.4(IL17RC):c.2092C>A (p.Pro698Thr)
NM_153460.4(IL17RC):c.2096C>T (p.Pro699Leu) rs1276617323
NM_153460.4(IL17RC):c.2107G>A (p.Ala703Thr)
NM_153460.4(IL17RC):c.2108C>A (p.Ala703Glu)
NM_153460.4(IL17RC):c.2110C>G (p.Pro704Ala) rs1036868156
NM_153460.4(IL17RC):c.2111C>G (p.Pro704Arg) rs1458109447
NM_153460.4(IL17RC):c.2112G>A (p.Pro704=) rs749233546
NM_153460.4(IL17RC):c.2117G>T (p.Arg706Leu) rs1385111108
NM_153460.4(IL17RC):c.2118C>T (p.Arg706=) rs1437448404
NM_153460.4(IL17RC):c.2122G>A (p.Val708Met) rs761099118
NM_153460.4(IL17RC):c.2132_2133insGGCGGGACCAGG (p.710PGAG[3]) rs1458271651
NM_153460.4(IL17RC):c.2133_2144del (p.710PGAG[1]) rs765314616
NM_153460.4(IL17RC):c.2147C>T (p.Ala716Val) rs867817700
NM_153460.4(IL17RC):c.2155G>C (p.Gly719Arg)
NM_153460.4(IL17RC):c.2161T>G (p.Ter721Glu)

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