Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11