Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9