Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34651
TNPO1
1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
rs1328599 10 95294018 upstream gene variant G/T snv 0.92 1
rs896322
LOC101929459 ; TMCC2
1 205240617 intron variant A/G snv 0.92 1
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs6449502
ELOVL7
5 60797268 intron variant T/C snv 0.82 1
rs7641175
TBC1D5
3 18269920 intron variant G/A snv 0.81 3
rs4777161
DRAIC
15 69569200 intron variant A/G snv 0.81 1
rs647316
EHD3
2 31241963 intron variant A/G snv 0.80 1
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs655029
EHD3
2 31254972 intron variant G/A snv 0.78 3
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs10506328
NFE2
12 54293448 intron variant A/C snv 0.75 1
rs2057149
DDO
6 110396290 intron variant C/T snv 0.74 2
rs477895
BAD ; GPR137
11 64281440 intron variant C/T snv 0.74 2
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs3215853
DOCK8
9 273178 intron variant -/A delins 0.72 1
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs4764487
LOC105369625 ; CD9
12 6223672 intron variant A/G snv 0.72 1
rs4849845
RALB
2 120255593 intron variant G/A snv 0.71 1
rs143636430
LRCH1
13 46668723 intron variant TGGCGGGGTGGCGGGG/-;TGGCGGGG;TGGCGGGGTGGCGGGGTGGCGGGG delins 0.71 1
rs2733310
TCF12
15 57206493 intron variant T/G snv 0.70 1
rs2546976 5 160173207 intergenic variant T/C snv 0.70 1
rs13257813 8 19167306 intron variant G/A snv 0.70 1
rs10876550
COPZ1
12 54318524 intron variant G/A snv 0.68 2