Bartter Syndrome

Other 59 variants 5 genes

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Associated Genes (5)
Associated Variants (59)
RSID Gene Risk Allele Odds Ratio Evidence
RS779747435 KCNJ1 — — strong
RS1180658535 CLCNKB — — strong
RS750710315 SLC12A3 — — strong
RS776210036 SLC12A3 — — strong
RS781209989 SLC12A3 — — strong
RS1007109925 BSND — — strong
RS200320892 KCNJ1 — — strong
RS764078087 KCNJ1 — — strong
RS1451284628 SLC12A3 — — strong
RS754523289 BSND — — strong
RS753949204 KCNJ1 — — strong
RS1465842300 SLC12A1 — — strong
RS764778741 KCNJ1 — — strong
RS755714542 CLCNKB — — strong
RS2041199779 SLC12A1 — — strong
RS1366101480 SLC12A1 — — strong
RS2042079691 SLC12A1 — — strong
RS770400317 SLC12A1 — — strong
RS201540273 CLCNKB — — strong
RS199877869 SLC12A1 — — strong
RS2497573845 KCNJ1 — — strong
RS2505190299 SLC12A1 — — strong
RS758128834 KCNJ1 — — strong
RS1301110174 BSND — — strong
RS2505087791 SLC12A1 — — strong
RS104894254 KCNJ1 — — strong
RS74315286 BSND — — strong
RS74315287 BSND — — strong
RS74315288 BSND — — strong
RS74315289 BSND — — strong
RS121908144 BSND — — strong
RS121909132 CLCNKB — — strong
RS121909136 CLCNKB — — strong
RS554794449 CLCNKB — — strong
RS1191726071 CLCNKB — — strong
RS121909380 SLC12A3 — — strong
RS104894246 KCNJ1 — — strong
RS104894253 KCNJ1 — — strong
RS74315285 BSND — — strong
RS754819005 BSND — — strong
RS138977195 SLC12A3 — — strong
RS180858237 BSND — — strong
RS141403253 BSND — — strong
RS200246335 BSND — — strong
RS747229048 SLC12A1 — — strong
RS147394986 BSND — — strong
RS143711308 BSND — — strong
RS373367600 KCNJ1 — — strong
RS781101708 BSND — — strong
RS750027126 BSND — — strong
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