Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 4
rs62524579 8 142979538 downstream gene variant G/A;C;T snv 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs11731886
LOC105377506
4 155738667 downstream gene variant A/C snv 0.21 3
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs751985
LRRC10B
11 61511118 downstream gene variant C/T snv 0.12 3
rs10628234 15 74918801 downstream gene variant -/CA delins 2
rs11486794 7 2452283 downstream gene variant C/T snv 0.14 2
rs12209106 6 1620807 downstream gene variant T/G snv 0.37 2
rs148871069
ADRA1B
5 159977464 downstream gene variant A/G snv 3.2E-03 2
rs16853958
LOC105371692
1 204559216 downstream gene variant A/C snv 0.59 2
rs2969070 7 2472910 downstream gene variant G/A;C snv 2
rs4507656 7 22116920 downstream gene variant C/G snv 0.27 2
rs6797587 3 48156124 downstream gene variant A/G;T snv 2
rs71647020 1 11918477 downstream gene variant G/A snv 3.4E-02 2
rs7497026 15 74916208 downstream gene variant T/C snv 0.46 2
rs76735299 8 141386381 downstream gene variant G/A;C snv 2
rs10228276
HOTTIP
7 27207660 downstream gene variant G/A snv 0.73 1
rs1081707 2 96381261 downstream gene variant G/A snv 0.24 1