Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7803454
PILRA
0.851 0.040 7 100393925 intron variant C/T snv 0.14 4
rs10895322
MMP20
0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 1
rs67538026
CNN2
0.851 0.040 19 1031439 intron variant C/T snv 0.37 4
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs12930861 1.000 0.040 16 10492245 upstream gene variant C/A;G;T snv 1
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs11184959 1.000 0.040 1 106671354 intergenic variant G/A snv 0.30 1
rs4698775
MCUB
1.000 0.040 4 109669323 intron variant G/A;T snv 1
rs2285714
PLA2G12A
0.882 0.040 4 109717654 synonymous variant C/T snv 0.37 0.31 1
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 4
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 4
rs7676999 1.000 0.040 4 116012923 intron variant C/T snv 0.16 1
rs1999930
FRK
0.882 0.040 6 116065971 intergenic variant C/A;G;T snv 1
rs3812111
NT5DC1 ; COL10A1
1.000 0.040 6 116122572 intron variant T/A snv 0.47 1
rs1064583
NT5DC1 ; COL10A1
0.925 0.040 6 116125413 missense variant A/C;G snv 0.37 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs17050244 1.000 0.040 2 120525054 regulatory region variant A/C;G snv 1
rs9482193
LOC105377979
1.000 0.040 6 121908390 intergenic variant G/T snv 0.58 1
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 4
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 3
rs10510110
PLEKHA1
0.925 0.120 10 122432914 3 prime UTR variant T/C snv 0.56 1