Channelopathy-associated Congenital Insensitivity to Pain

Other 85 variants 1 gene

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Associated Genes (1)

SCN9A

Associated Variants (85)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS201915876	SCN9A	—	—	strong
RS200070962	SCN9A	—	—	strong
RS200956485	SCN9A	—	—	strong
RS199784484	SCN9A	—	—	strong
RS763256222	SCN9A	—	—	strong
RS769971743	SCN9A	—	—	strong
RS199822303	SCN9A	—	—	strong
RS199572382	SCN9A	—	—	strong
RS202211795	SCN9A	—	—	strong
RS372210358	SCN9A	—	—	strong
RS1018959938	SCN9A	—	—	strong
RS765818027	SCN9A	—	—	strong
RS200780217	SCN9A	—	—	strong
RS1553478584	SCN9A	—	—	strong
RS569406301	SCN9A	—	—	strong
RS1024152367	SCN9A	—	—	strong
RS369148683	SCN9A	—	—	strong
RS1553495048	SCN9A	—	—	strong
RS1323162486	SCN9A	—	—	strong
RS201560701	SCN9A	—	—	strong
RS2106527836	SCN9A	—	—	strong
RS2106493110	SCN9A	—	—	strong
RS2468067609	SCN9A	—	—	strong
RS2468024864	SCN9A	—	—	strong
RS2467868979	SCN9A	—	—	strong
RS201990547	SCN9A	—	—	strong
RS180922748	SCN9A	—	—	strong
RS200163716	SCN9A	—	—	strong
RS188336294	SCN9A	—	—	strong
RS71428908	SCN9A	—	—	strong
RS794729216	SCN9A	—	—	strong
RS79805025	SCN9A	—	—	strong
RS201184093	SCN9A	—	—	strong
RS200625860	SCN9A	—	—	strong
RS201875421	SCN9A	—	—	strong
RS202047865	SCN9A	—	—	strong
RS201984007	SCN9A	—	—	strong
RS188145203	SCN9A	—	—	strong
RS199550149	SCN9A	—	—	strong
RS755653914	SCN9A	—	—	strong
RS200415928	SCN9A	—	—	strong
RS200560768	SCN9A	—	—	strong
RS202152511	SCN9A	—	—	strong
RS780673293	SCN9A	—	—	strong
RS367794835	SCN9A	—	—	strong
RS1553473041	SCN9A	—	—	strong
RS200610689	SCN9A	—	—	strong
RS759003928	SCN9A	—	—	strong
RS766212849	SCN9A	—	—	strong
RS202002028	SCN9A	—	—	strong

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