Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 1
rs374039502
TNFSF13B
0.925 0.160 13 108308037 3 prime UTR variant T/A snv 2.0E-02 1
rs4622308 0.925 0.160 12 56075401 upstream gene variant C/T snv 1
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 1
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 1
rs934734
SPRED2
0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 1
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 1
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs10937560
MB21D2
0.882 3 192909627 intron variant G/C snv 0.45 4
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4