Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114846969 19 11080521 downstream gene variant G/A snv 0.12 1
rs217386 7 44561096 downstream gene variant G/A snv 0.41 1
rs2294261 6 16108932 downstream gene variant A/C snv 0.65 1
rs4002471 19 48711838 downstream gene variant C/T snv 0.39 1
rs72834327 2 117842293 downstream gene variant A/T snv 5.7E-02 1
rs75214121 8 58485717 downstream gene variant C/T snv 2.5E-02 1
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 6
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 6
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 4
rs5014650 6 160678471 upstream gene variant G/A snv 0.16 4
rs821840
CETP
16 56959974 upstream gene variant A/G snv 4
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 3
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 3
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 3
rs17725246
NPC1L1
7 44542387 upstream gene variant T/A;C snv 3
rs56204645
RP1
8 54509209 upstream gene variant T/C snv 0.19 3