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: rs1799750
rs1799750
48 0.592 0.760 11 102799765 intron variant C/- delins 0.50 0.010 < 0.001 1 2016 2016
dbSNP: rs2071230
rs2071230
3 0.882 0.080 11 102790228 3 prime UTR variant A/G snv 0.15 0.010 1.000 1 2012 2012
dbSNP: rs773474756
rs773474756
2 0.925 0.080 11 102790467 missense variant T/C snv 8.1E-06 0.010 1.000 1 2012 2012