Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 2
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs11602954
BET1L
11 202856 intron variant G/A snv 0.17 2
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 2
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 2
rs2297067
EXOC3L4
1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 2
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 2
rs513349
GGNBP1 ; BAK1
1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 2
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 2
rs399604
HLA-DOA
1.000 0.120 6 33007237 non coding transcript exon variant T/C snv 0.40 0.40 2
rs3809114
INHBE
0.925 0.120 12 57454856 5 prime UTR variant G/A snv 0.44 2
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 2
rs4379723
JMJD1C
10 63203689 intron variant T/C snv 0.43 2
rs10974808
RCL1
9 4840380 intron variant A/G snv 9.0E-02 2
rs1668871
TMCC2
1 205268009 intron variant T/C;G snv 2
rs8109288
TPM4
19 16074749 non coding transcript exon variant G/A snv 3.9E-02 2
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 2
rs7961894
WDR66
12 121927677 intron variant C/T snv 7.3E-02 2
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 2
rs11628318 14 102573750 regulatory region variant T/A;C snv 1
rs13042885 20 1944061 upstream gene variant C/A;T snv 1
rs1719271 15 64891602 intron variant A/G snv 0.20 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1