Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4360494
SF3A3
0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 9
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6