rs771316846, CLCNKB

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Gitelman Syndrome
CUI: C0268450
Disease: Gitelman Syndrome
120 0.925 0.160 1 16045636 missense variant T/C snv 8.0E-06 0.020 1.000 2 2008 2016
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.160 1 16045636 missense variant T/C snv 8.0E-06 0.010 1.000 1 2009 2009