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: rs3761959
rs3761959
1 0.827 0.320 1 157699488 intron variant C/A;G;T snv 0.810 1.000 1 2011 2013
dbSNP: rs7522061
rs7522061
1 0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 0.700 1.000 1 2011 2011