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: rs10006237
rs10006237
1 4 136606920 intergenic variant C/T snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10009397
rs10009397
1 4 28695228 intergenic variant A/T snv 0.89 0.700 1.000 1 2018 2018
dbSNP: rs10009715
rs10009715
1 4 171510209 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10026457
rs10026457
1 4 58384912 intergenic variant T/G snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs10040865
rs10040865
1 5 171411280 downstream gene variant G/A snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs10055216
rs10055216
1 5 170981562 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10057590
rs10057590
1 5 124999554 intron variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10061387
rs10061387
1 5 124524355 intron variant A/G snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs10064431
rs10064431
1 5 93614967 downstream gene variant T/C snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs10065159
rs10065159
1 5 172668864 intron variant T/C snv 0.77 0.700 1.000 1 2018 2018
dbSNP: rs10066711
rs10066711
1 5 88894787 intron variant A/T snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs10073038
rs10073038
1 5 111230823 intron variant A/T snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs1007966
rs1007966
1 9 89599052 non coding transcript exon variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10088255
rs10088255
1 8 102355371 intron variant A/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs10106406
rs10106406
1 8 140996099 intron variant C/A;G snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs10107533
rs10107533
1 8 19521910 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10109012
rs10109012
1 8 15387338 intergenic variant C/T snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs1011392
rs1011392
1 18 55374672 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs10114066
rs10114066
1 9 73908824 intergenic variant T/A snv 0.76 0.700 1.000 1 2018 2018
dbSNP: rs10122976
rs10122976
1 9 135751066 intron variant C/A;T snv 0.47; 1.2E-05 0.700 1.000 1 2018 2018
dbSNP: rs10132779
rs10132779
1 14 29249690 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10136545
rs10136545
1 14 54886145 non coding transcript exon variant C/T snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs10137343
rs10137343
1 14 22913431 intron variant A/T snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs1015438
rs1015438
1 16 51143606 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1016162
rs1016162
1 3 102299 regulatory region variant C/T snv 0.36 0.700 1.000 1 2018 2018