Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 8
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 4
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 3
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 2
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 2
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 2
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 2
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 1
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 1
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 1
rs3740393
BORCS7-ASMT ; AS3MT
0.776 0.280 10 102876898 intron variant G/C;T snv 1
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 1
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 3
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 1
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 6
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 2
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 2
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 23
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 14