Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9356181
LOC105378102
6 164055994 intergenic variant C/A snv 0.51 1
rs169219 6 25957164 intergenic variant C/A;G snv 3
rs4466998
MAX ; CHURC1-FNTB ; FNTB
14 65008822 intron variant C/A;G snv 2
rs643381 6 139518286 intron variant C/A;G snv 2
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs12718597
IKZF1
7 50360730 intron variant C/A;T snv 2
rs9859260
TFRC
3 196073676 intron variant C/A;T snv 2
rs12135894 1 3811497 downstream gene variant C/A;T snv 1
rs2572207
DENND4A ; RAB11A
15 65778355 intron variant C/A;T snv 1
rs172629 4 54541595 intergenic variant C/G snv 0.17 2
rs218256 4 54536242 intergenic variant C/G snv 0.38 2
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 4
rs837763
LOC107984842
16 88787321 upstream gene variant C/G;T snv 2
rs6538148 12 88424702 intergenic variant C/G;T snv 1
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 4
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 4
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs218237 4 54528005 intergenic variant C/T snv 0.18 4