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: rs2569190
rs2569190
39 0.620 0.560 5 140633331 intron variant A/G snv 0.57 0.010 1.000 1 2010 2010
dbSNP: rs2569191
rs2569191
2 1.000 0.080 5 140634318 upstream gene variant C/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs4914
rs4914
2 0.925 0.160 5 140631883 synonymous variant C/A;G snv 4.8E-05; 9.3E-02 0.010 1.000 1 2010 2010
dbSNP: rs5744455
rs5744455
5 0.882 0.160 5 140633722 upstream gene variant G/A;T snv 0.010 1.000 1 2010 2010