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
rs10094872
CASC11
0.882 0.200 8 127707639 intron variant A/T snv 0.33 3
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
rs4510656
CDKAL1
0.925 0.120 6 20766466 intron variant C/A snv 0.39 2
rs5003154
PAG1
0.925 0.120 8 81074718 intron variant T/C;G snv 2
rs6104690
LINC02871
0.925 0.120 20 11007451 intron variant G/A;T snv 2
rs62185668 0.925 0.120 20 10981287 intron variant C/A snv 0.19 2
rs7238033
SLC14A1 ; LOC105372093
0.925 0.120 18 45737001 intron variant T/C snv 0.61 2
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 2
rs7747724
CDKAL1
0.925 0.120 6 20751084 intron variant T/C snv 0.41 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
rs17650301
POLG2 ; MILR1
0.925 0.120 17 64483156 intron variant A/C snv 0.23 1
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 1
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 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
rs4813953
LINC02871
1.000 0.120 20 11010490 intron variant T/C snv 0.63 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