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: rs10080237
rs10080237
1 6 80144753 intron variant T/C snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs10101061
rs10101061
1 8 23735787 intron variant T/A snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs10132280
rs10132280
6 14 25458973 intergenic variant C/A snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs10195252
rs10195252
7 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs10231365
rs10231365
1 7 20391962 intron variant C/T snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs10408163
rs10408163
6 19 47093845 non coding transcript exon variant T/C snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs10429950
rs10429950
3 1.000 0.040 1 218451191 intergenic variant T/C snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs1043595
rs1043595
2 7 128769958 3 prime UTR variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1046934
rs1046934
4 1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs10482795
rs10482795
2 1 218432267 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10510554
rs10510554
2 3 25058285 intron variant T/C snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs1055144
rs1055144
3 1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs10786152
rs10786152
1 10 94133757 intron variant A/G snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs10804591
rs10804591
5 3 129615390 intergenic variant C/A snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs10842707
rs10842707
4 12 26318431 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10842708
rs10842708
2 12 26321934 intron variant G/A snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs10843151
rs10843151
1 12 28318386 intron variant G/A snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs10849145
rs10849145
1 12 4808002 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs10876528
rs10876528
2 12 54027692 intron variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10919388
rs10919388
4 1 170403362 intergenic variant A/C snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs10923712
rs10923712
4 1 118962811 intron variant G/A snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs10923724
rs10923724
3 1 119004219 upstream gene variant C/T snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs10938397
rs10938397
19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs10946808
rs10946808
5 1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10968577
rs10968577
3 9 28415514 intron variant C/T snv 0.27 0.700 1.000 1 2017 2017