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: rs1180243
rs1180243
ME1
1 1.000 6 83213997 intron variant G/T snv 0.51 0.010 1.000 1 2010 2010
dbSNP: rs2071373
rs2071373
1 1.000 2 112782507 intron variant G/A snv 0.74 0.010 1.000 1 2010 2010
dbSNP: rs315921
rs315921
1 1.000 2 113114474 intron variant G/A snv 0.12 0.010 1.000 1 2010 2010
dbSNP: rs315934
rs315934
1 1.000 2 113126129 intron variant T/C snv 0.15 0.010 1.000 1 2010 2010
dbSNP: rs315946
rs315946
1 1.000 2 113136287 downstream gene variant G/A snv 9.6E-02 0.010 1.000 1 2010 2010