Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7811142
TSC22D4
7 100467820 synonymous variant A/C;T snv 0.16 1
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs7149242 14 100693079 intergenic variant T/G snv 0.62 1
rs9635298 14 100706205 regulatory region variant C/T snv 0.13 1
rs1555405 14 100710432 regulatory region variant G/A snv 0.29 2
rs72635188
ZNF839
14 102319464 5 prime UTR variant G/T snv 9.6E-02 1
rs1190545
TECPR2
14 102437842 intron variant G/A;C;T snv 1
rs11628318 14 102573750 regulatory region variant T/A;C snv 1
rs10132160
RCOR1
14 102591686 upstream gene variant A/G snv 0.80 1
rs11382616
RCOR1
14 102615129 intron variant C/-;CC;CCC;CCCC;CCCCC delins 1
rs2297067
EXOC3L4
1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 2
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 3
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs4846217 1 10391742 upstream gene variant C/T snv 0.14 1
rs4699154 4 105112927 intron variant T/A;C snv 2
rs2816648
BRF1
14 105241952 5 prime UTR variant C/T snv 0.23 1
rs112790992
BRF1
14 105291880 intron variant A/C snv 0.31 1
rs2343592
ZFPM2 ; ZFPM2-AS1
8 105560042 intron variant A/G snv 0.30 1
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs553314025
AP1M2
19 10576094 intron variant TT/-;T;TTT;TTTT;TTTTT delins 1
rs2360742
SLC44A2
19 10629898 intron variant T/C;G snv 1
rs342213
CTB-30L5.1
7 106684166 intron variant G/C snv 0.37 1
rs342275
CTB-30L5.1
7 106718770 intron variant C/T snv 0.33 1
rs67036916
CTB-30L5.1
7 106727190 intron variant G/A snv 0.36 1
rs342292
CTB-30L5.1
7 106730198 intron variant C/G snv 0.40 1