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: rs1057519749
rs1057519749
1 1.000 0.040 21 34880579 missense variant C/A;G snv 0.700 1.000 3 2014 2014
dbSNP: rs1057519750
rs1057519750
1 1.000 0.040 21 34880580 missense variant C/T snv 0.700 1.000 2 2009 2014
dbSNP: rs1057519748
rs1057519748
5 0.827 0.120 21 34859486 stop gained G/A snv 0.700 1.000 1 1999 1999
dbSNP: rs1482518887
rs1482518887
8 0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs2249650
rs2249650
1 1.000 0.040 21 34808689 intron variant A/G snv 0.51 0.010 1.000 1 2016 2016
dbSNP: rs2268276
rs2268276
2 0.925 0.040 21 34808717 intron variant G/A snv 0.38 0.010 1.000 1 2016 2016
dbSNP: rs74315450
rs74315450
5 0.851 0.120 21 34859485 missense variant C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs757412228
rs757412228
2 0.925 0.080 21 34886917 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2016 2016