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: rs2237892
rs2237892
KCNQ1
16 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 0.900 1.000 32 2008 2019