Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs1053872
RCL1
0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv 2
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 2
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 2
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 2
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 2
rs2075555
COL1A1
0.807 0.240 17 50196930 intron variant T/A;G snv 2
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 2
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2