Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10048745
ARHGAP25
2 68735005 5 prime UTR variant G/A snv 0.24 2
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31 2
rs1006409
LOC100506606 ; FAR2
12 29282742 non coding transcript exon variant A/G snv 0.51 1
rs10075570
RNF145
5 159172350 intron variant G/A;T snv 1
rs10132160
RCOR1
14 102591686 upstream gene variant A/G snv 0.80 1
rs10199109
LOC105373583
2 120236957 upstream gene variant G/T snv 0.75 1
rs10220411
ACTN1-AS1
14 68985371 intron variant A/G snv 0.29 2
rs1034564
ARVCF
22 19996490 intron variant C/T snv 0.24 1
rs1034566
ARVCF
22 19996754 intron variant C/G;T snv 1
rs10431427
MRPL42
12 93489363 intron variant C/T snv 0.37 1
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 2
rs10512472
SLFN14
17 35557785 missense variant T/C snv 0.21 0.19 1
rs10514301
LINC00461
5 88643836 intron variant C/T snv 0.16 2
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs1060431
SLC25A11
17 4937573 3 prime UTR variant G/A snv 0.13 2
rs10654220
MPHOSPH9
1.000 0.040 12 123218875 intron variant -/TGT;TGTTGT delins 2
rs10661645
NAA25
12 112086916 intron variant -/GAG;GGAG delins 0.95 1
rs10757287 9 22143571 regulatory region variant A/T snv 0.22 1
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs10769960
LOC102724784 ; DENND2B
11 8797456 intron variant T/C snv 0.34 1
rs10811664 9 22142908 regulatory region variant G/A snv 0.21 1
rs10820606 9 96430637 intergenic variant A/C snv 0.23 2