Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11670056
ELL
1.000 0.040 19 18479133 intron variant C/T snv 5.2E-02 2
rs11673093
EXOC3L2 ; MARK4
1.000 0.040 19 45238836 synonymous variant G/A snv 0.22 2
rs12315434
R3HDM2
1.000 0.040 12 57387153 intron variant A/C snv 0.16 2
rs13734
RRBP1
1.000 0.040 20 17614084 3 prime UTR variant G/A snv 0.15 2
rs147555597
LPAL2
1.000 0.040 6 160490564 intron variant G/A snv 5.5E-03 2
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 2
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12 2
rs17228058
SMAD3
1.000 0.040 15 67157967 intron variant A/G snv 0.17 2
rs2071382
FES
1.000 0.040 15 90884967 intron variant T/C snv 0.57 2
rs2074158
DHX58
1.000 0.040 17 42105145 missense variant T/C snv 0.21 0.33 2
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 2
rs216172
SMG6
0.925 0.040 17 2223210 intron variant G/C snv 0.35 2
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 2
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 2
rs2814993
ILRUN
1.000 0.040 6 34651116 intron variant G/A snv 0.17 2
rs34991912
FGD5
1.000 0.040 3 14884844 intron variant T/A;C snv 2
rs35237252 1.000 0.040 8 20012760 intergenic variant C/A;T snv 0.24 2
rs35489971
CD300LF ; RAB37
1.000 0.040 17 74704804 missense variant A/G;T snv 0.73 2
rs3741782
CORO1C
1.000 0.040 12 108701361 intron variant A/G;T snv 0.31; 4.0E-06 2
rs3745348
MYO9B
1.000 0.040 19 17101600 intron variant C/T snv 0.38 2
rs3895874
GIP
1.000 0.040 17 48970506 upstream gene variant G/A;C snv 2
rs41269133 1.000 0.040 6 160666831 intron variant T/C snv 8.8E-02 2
rs41272114
LPA
1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02 2
rs4252185
PLG
1.000 0.040 6 160702419 intron variant T/C snv 5.7E-02 2
rs472109
SWAP70
1.000 0.040 11 9748771 intron variant G/C;T snv 2