Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs34651
TNPO1
1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 4
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs11601507
TRIM5
1.000 0.040 11 5679844 missense variant C/A;T snv 9.3E-02; 4.0E-06 3
rs1473247
RNF145
1.000 0.040 5 159176563 intron variant T/C snv 0.41 2
rs649729
EHD3
1.000 0.040 2 31241519 intron variant T/A;C snv 2
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 1
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 2
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 1
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 3
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 2
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 2
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs7539542
ADIPOR1
0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58 1
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 3