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: rs750414160
rs750414160
KCNJ11
2 0.925 0.120 11 17387224 missense variant C/A;T snv 4.0E-06; 2.0E-05 0.010 1.000 1 2011 2011
dbSNP: rs769279368
rs769279368
ABCC8
2 0.925 0.120 11 17395872 missense variant C/A;T snv 3.9E-05 0.010 1.000 1 2001 2001