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: rs387906930
rs387906930
WFS1
8 0.790 0.360 4 6301846 missense variant C/G;T snv 0.800 1.000 3 2006 2011
dbSNP: rs387906931
rs387906931
WFS1
2 0.925 0.360 4 6302133 missense variant G/A snv 0.800 1.000 3 2006 2011
dbSNP: rs74315205
rs74315205
WFS1 ; LOC107986257
7 0.807 0.360 4 6302385 missense variant G/A snv 0.800 1.000 3 2006 2011
dbSNP: rs71539673
rs71539673
WFS1
2 0.925 0.320 4 6302220 missense variant G/A snv 0.710 1.000 1 2016 2016
dbSNP: rs876657675
rs876657675
WFS1
1 1.000 0.320 4 6302303 missense variant G/C snv 0.700 0