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: rs1008878
rs1008878
2 1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs10115049
rs10115049
2 1.000 0.040 9 22032120 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs10120688
rs10120688
7 0.807 0.080 9 22056500 intron variant G/A snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs10217586
rs10217586
2 1.000 0.040 9 22121350 intron variant A/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10738604
rs10738604
3 1.000 0.040 9 22025494 intron variant G/A snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs10738605
rs10738605
3 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10738606
rs10738606
2 1.000 0.040 9 22088091 intron variant A/T snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs10757264
rs10757264
2 1.000 0.040 9 22019733 intron variant A/G snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs10757265
rs10757265
2 1.000 0.040 9 22048860 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs10757267
rs10757267
2 1.000 0.040 9 22052811 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10757270
rs10757270
2 1.000 0.040 9 22072720 intron variant A/C;G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10757277
rs10757277
2 1.000 0.040 9 22124451 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10757279
rs10757279
3 0.925 0.040 9 22124631 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10811641
rs10811641
2 1.000 0.040 9 22014138 non coding transcript exon variant C/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs10811643
rs10811643
2 1.000 0.040 9 22024967 intron variant A/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10811645
rs10811645
2 1.000 0.040 9 22049657 intron variant G/A snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs10811656
rs10811656
7 0.807 0.200 9 22124473 intron variant C/T snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs10965212
rs10965212
3 0.925 0.080 9 22023796 intron variant T/A;C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10965215
rs10965215
4 0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 0.700 1.000 1 2013 2013
dbSNP: rs10965219
rs10965219
4 0.882 0.080 9 22053688 intron variant A/G snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs1333036
rs1333036
2 1.000 0.040 9 22043820 intron variant T/C snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs1333037
rs1333037
3 0.925 0.040 9 22040766 intron variant C/T snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs1333040
rs1333040
15 0.732 0.280 9 22083405 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1333045
rs1333045
14 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 0.700 1.000 1 2011 2011