Pseudohypoaldosteronism

Other 122 variants 3 genes

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Associated Genes (3)
Associated Variants (122)
RSID Gene Risk Allele Odds Ratio Evidence
RS2497885818 SCNN1A — — strong
RS139012605 SCNN1G — — strong
RS72647546 SCNN1G — — strong
RS146413363 SCNN1G — — strong
RS564570566 SCNN1B — — strong
RS765336896 SCNN1B — — strong
RS200966246 SCNN1B — — strong
RS201369319 SCNN1B — — strong
RS146440372 SCNN1B — — strong
RS13306627 SCNN1B — — strong
RS747116196 SCNN1B — — strong
RS2142020387 SCNN1B — — strong
RS2136865918 SCNN1A — — strong
RS774767092 SCNN1G — — strong
RS367681929 SCNN1A — — strong
RS2497930442 SCNN1A — — strong
RS1962240610 SCNN1B — — strong
RS200557019 SCNN1A — — strong
RS908355642 SCNN1B — — strong
RS2506496434 SCNN1B — — strong
RS2506410452 SCNN1B — — strong
RS2506496921 SCNN1B — — strong
RS201318322 SCNN1B — — strong
RS372956932 SCNN1A — — strong
RS372994709 SCNN1B — — strong
RS1369791519 SCNN1A — — strong
RS541449814 SCNN1B — — strong
RS142439390 SCNN1A — — strong
RS144653364 SCNN1G — — strong
RS1182475940 SCNN1B — — strong
RS201873521 SCNN1A — — strong
RS149868979 SCNN1B — — strong
RS1565488675 SCNN1A — — strong
RS771949339 SCNN1A — — strong
RS138995556 SCNN1A — — strong
RS61729789 SCNN1B — — strong
RS148959452 SCNN1A — — strong
RS200770604 SCNN1A — — strong
RS200714599 SCNN1B — — strong
RS1565478701 SCNN1A — — strong
RS1596760831 SCNN1G — — strong
RS536187488 SCNN1B — — strong
RS146420892 SCNN1G — — strong
RS550424284 SCNN1B — — strong
RS140681881 SCNN1A — — strong
RS539360032 SCNN1A — — strong
RS751903373 SCNN1A — — strong
RS755287192 SCNN1A — — strong
RS369382063 SCNN1A — — strong
RS1366336758 SCNN1A — — strong
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