Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554700718
HNRNPK
0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs886040971
TRPS1
0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs587784347
PLA2G6
0.742 0.280 22 38113561 missense variant G/A snv 8.0E-06 38
rs1441937959
EFL1
0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 19
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 17
rs1114167422
SNORA56 ; DKC1
0.776 0.320 X 154773148 missense variant A/G snv 11
rs386834070
VPS13B
0.851 0.360 8 99134644 stop gained C/T snv 9
rs782596945
ATP2B3
0.851 0.120 X 153580229 missense variant G/A;T snv 5.5E-06 8
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 5
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 4
rs10851907
CHRNB4
1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 4
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 2
rs80356779
CPT1A
0.776 0.320 11 68780662 missense variant G/A snv 3.2E-05 5.6E-05 2
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 2
rs149467613
P2RY2
1.000 0.040 11 73232438 intron variant G/A snv 3.3E-02 2
rs931608
ZNF98
1.000 0.040 19 22431320 intron variant A/C;T snv 2
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs10811723 1.000 0.040 9 22542286 intergenic variant A/G snv 0.55 1
rs1108343 1.000 0.040 16 51177684 non coding transcript exon variant T/C snv 0.52 1
rs11166135 1.000 0.040 1 98883280 intergenic variant A/G snv 0.10 1