Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs10137082
IL25
0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 2
rs10178409 1.000 0.080 2 73628380 downstream gene variant G/T snv 0.26 2
rs1020120
LOC102724036
1.000 0.080 9 84611173 intron variant C/T snv 0.60 2
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs102274
TMEM258
1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28 3
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs10404257
ACTN4
0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 2
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 3
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1066621 1.000 0.080 3 191708066 regulatory region variant C/T snv 0.39 2
rs10774021
SLC6A13
1.000 0.080 12 240132 intron variant C/T snv 0.57 4
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3
rs10783124 1.000 0.080 1 99937719 intergenic variant A/G snv 2.9E-02 1
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 4
rs10808565
PVT1
0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 2