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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 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
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4