Bartter Syndrome
Other
59 variants
5 genes
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Associated Genes (5)
KCNJ1
CLCNKB
SLC12A3
BSND
SLC12A1
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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