Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
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
rs80358079
BRCA1
0.827 0.200 17 43057147 intron variant C/T snv 6
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
rs2981575
FGFR2
0.882 0.120 10 121586602 intron variant G/A snv 0.54 4