Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs201540273
rs201540273
CLCNKB
2 0.925 0.160 1 16051725 missense variant G/A snv 2.4E-05 7.7E-05 0.010 1.000 1 2003 2003