Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35041767
PTPRD
1.000 0.080 9 9261737 intron variant -/C ins 1
rs1820989 1.000 0.080 2 67842758 intergenic variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1836229
PTPRD
1.000 0.080 9 8820573 intron variant A/C;G;T snv 1
rs3810651
GABRQ ; LOC105373370
0.925 0.080 X 152652814 missense variant A/C;T snv 4
rs2280673
RAB6B
0.882 0.160 3 133839310 intron variant A/C;T snv 3
rs6904723
BTBD9
1.000 0.080 6 38468541 intron variant A/C;T snv 1
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs12469063
MEIS1
0.925 0.080 2 66537176 intron variant A/G snv 0.18 2
rs12593813
MAP2K5
1.000 0.080 15 67744514 intron variant A/G snv 0.53 2
rs10208712 1.000 0.080 2 3986856 regulatory region variant A/G snv 0.26 1
rs11635424
MAP2K5
1.000 0.080 15 67745240 intron variant A/G snv 0.53 1
rs17636328
LINC02520
1.000 0.080 6 37522755 intron variant A/G snv 0.14 1
rs35987657
LOC105374107 ; LOC107986023
1.000 0.080 3 130816723 upstream gene variant A/G snv 0.29 1
rs365032
MYT1
1.000 0.080 20 64164052 intron variant A/G snv 0.26 1
rs3923809
BTBD9
1.000 0.080 6 38473194 intron variant A/G snv 0.32 1
rs6747972 1.000 0.080 2 67843093 intergenic variant A/G snv 0.65 1
rs7881785 1.000 0.080 X 42995357 upstream gene variant A/G snv 1
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs1830084
SRPRB ; LOC105374116 ; TF
0.882 0.160 3 133789620 3 prime UTR variant A/G;T snv 4
rs10952927
LOC107986816
1.000 0.080 7 88729746 intron variant A/G;T snv 1
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs1848460 1.000 0.080 3 3406460 intron variant A/T snv 0.33 1