Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 4
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 3
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 3
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 2
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 2
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 2
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 2
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 2
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 1
rs11175194
SRGAP1
0.925 0.120 12 63871057 intron variant G/A snv 0.15 1
rs115344852
GPX6
1.000 0.120 6 28518321 intron variant A/C snv 1
rs12039431
RSPO1
1.000 0.120 1 37616450 intron variant G/A snv 0.24 0.21 1
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 1
rs17130142
PKN2-AS1
1.000 0.120 1 87773925 intron variant G/A snv 6.5E-02 1
rs17329882
SYNPO2
0.925 0.120 4 119028805 intron variant A/C;T snv 1
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 1
rs3820282
LOC105376845 ; WNT4
0.925 0.120 1 22141722 intron variant C/T snv 0.13 1
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 1
rs4525119
LOC107984198 ; AKR1C3
0.925 0.120 10 5049762 intron variant C/T snv 0.30 1
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs74917072
UBE2F ; UBE2F-SCLY
0.882 0.120 2 238022053 intron variant G/A;T snv 1
rs7643459
LOC101927394 ; LMCD1-AS1
0.925 0.120 3 7963141 intron variant G/C;T snv 1