ClinVar Miner

List of variants in gene combination IL17RC, LOC129936144 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: 6
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HGVS dbSNP gnomAD frequency
NM_153460.4(IL17RC):c.2022C>T (p.Ser674=) rs757894385 0.00008
NM_153460.4(IL17RC):c.2028G>A (p.Arg676=) rs2125321875
NM_153460.4(IL17RC):c.2043G>A (p.Ala681=)
NM_153460.4(IL17RC):c.2067G>A (p.Gln689=) rs2125322609
NM_153460.4(IL17RC):c.2076G>A (p.Leu692=)
NM_153460.4(IL17RC):c.2118C>T (p.Arg706=) rs1437448404

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