Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6969780
HOXA-AS2 ; HOXA3
7 27119517 splice region variant G/A;C snv 4
rs891511
NOS3
7 151007755 intron variant G/A;C snv 4
rs1027989
LYN
8 55901862 intron variant G/A;C snv 3
rs11953630 5 158418394 intergenic variant C/A;T snv 3
rs11977526
LOC102723446
7 45968511 intron variant G/A;T snv 3
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 3
rs2004776
AGT
1 230712956 intron variant C/G;T snv 3
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 3
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 3
rs35529250
RBM47
4 40426074 missense variant C/G;T snv 1.2E-05; 3.7E-03 3
rs4373814 10 18131043 intergenic variant G/C;T snv 3
rs4462906 3 27551369 upstream gene variant T/A;G snv 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 3
rs7006531 8 94098516 intron variant A/C;G snv 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs7690819 1.000 0.040 4 111199502 intergenic variant A/G;T snv 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs78192203
GPR20
8 141364973 intron variant T/A;C snv 3
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 2