Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8105637
TINCR
0.925 0.120 19 5566221 intron variant A/G snv 0.56 2
rs9302752 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 2
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs3816527
PTX3 ; VEPH1
0.882 0.160 3 157437525 missense variant C/A snv 0.64 0.64 9
rs746429
SIPA1
0.882 0.120 11 65649963 synonymous variant G/A snv 0.31 0.30 8
rs11539752
LOC107984667 ; GZMB
0.882 0.120 14 24632383 missense variant G/C snv 0.21 0.26 6
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 6
rs61573157
ADAMTS14
0.882 0.160 10 70760503 missense variant C/T snv 8.6E-02 7.5E-02 6
rs6691378
CHI3L1
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19 6
rs10491121
LOC101927369 ; CCL4
0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs2881766
ESR1
0.882 0.120 6 151797984 intron variant T/G snv 0.35 5
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs2071504
POLR2A
0.882 0.120 17 7502618 non coding transcript exon variant C/T snv 0.18 0.17 4
rs2105269
GALNT16
0.882 0.120 14 69280517 intron variant A/G snv 0.35 4
rs3218038
CCNE1
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02 4
rs3917356
IL1B
0.882 0.160 2 112834786 intron variant C/T snv 0.39 4
rs438034
CENPF
0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs4719839
LOC105375199 ; LOC105375200
0.882 0.120 7 25946953 downstream gene variant G/A;C snv 4
rs6720283
COL6A3
0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs738722
CHEK2
0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs10754339
VTCN1
0.882 0.120 1 117147650 3 prime UTR variant G/A snv 0.88 0.76 3
rs1256054
ESR2
0.882 0.120 14 64249595 synonymous variant G/C snv 2.8E-03 9.6E-04 3
rs1455751791
ESR1
0.882 0.120 6 152011735 synonymous variant C/G snv 4.0E-06 3
rs17530068
LOC105377871
0.882 0.120 6 81483392 intergenic variant T/C snv 0.19 3