Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 9
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 9
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 7
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 6
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 5
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 5
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 4
rs2725207
PKD2
0.882 0.200 4 88058377 intron variant C/A snv 0.31 4
rs2981575
FGFR2
0.882 0.120 10 121586602 intron variant G/A snv 0.54 4
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 4
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 4
rs3784099
RAD51B
0.807 0.320 14 68283210 intron variant G/A snv 0.43 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 4
rs4971059
TRIM46
0.851 0.200 1 155176305 intron variant G/A snv 0.34 4