Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs1260236 1.000 0.040 9 6023030 intergenic variant A/G snv 2
rs12910524 1.000 0.040 15 101262360 intergenic variant T/A;C snv 2
rs1543654 1.000 0.040 21 34426752 upstream gene variant T/C snv 2
rs181914932 1.000 0.040 20 45932640 non coding transcript exon variant T/C snv 1.6E-02 2
rs2863389 1.000 0.040 3 166431104 intergenic variant C/T snv 0.17 2
rs4258701 1.000 0.040 18 27895834 intergenic variant C/T snv 0.28 2
rs57922 1.000 0.040 5 74282114 intron variant C/T snv 0.40 2
rs649529 1.000 0.040 11 88275083 intergenic variant G/A;T snv 2
rs6688849 1.000 0.040 1 47530532 intergenic variant A/C;G snv 2
rs6706313 1.000 0.040 2 60311754 regulatory region variant A/G snv 0.18 2
rs148529020
ABCC8
1.000 0.040 11 17460613 missense variant C/T snv 1.2E-05 1.4E-05 2
rs756823374
ABCC8
1.000 0.040 11 17463515 missense variant G/A snv 1.4E-05 2
rs181914721
ADAMTSL3
1.000 0.040 15 83819856 missense variant G/A snv 3.7E-04 1.2E-04 2
rs17791685
APPL1 ; ASB14 ; LOC105377102
1.000 0.040 3 57272583 3 prime UTR variant C/A snv 0.19 2
rs15673
ARSG ; SLC16A6
1.000 0.040 17 68267123 3 prime UTR variant C/A;T snv 7.0E-06 2
rs528035
ASB14
1.000 0.040 3 57289142 intron variant A/G snv 0.48 0.37 2
rs1042488900
ATF6
1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs1060366
ATP1A1
1.000 0.040 1 116384040 synonymous variant A/G snv 1.3E-03 1.4E-03 2
rs575152
ATP9B
1.000 0.040 18 79124480 intron variant C/T snv 0.14 2
rs1042615
AVPR1A
1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
rs10747983
AVPR1A
1.000 0.040 12 63144678 3 prime UTR variant G/A snv 0.29 2
rs56381858
CD36
1.000 0.040 7 80671994 stop gained T/C;G snv 4.0E-06; 2.4E-04 2
rs768883824
CD36
1.000 0.040 7 80666481 missense variant A/G snv 4.0E-06 2