Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72755295
EXO1
1.000 0.080 1 241870961 intron variant A/G snv 2.1E-02 3
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs111759324 1 101186966 upstream gene variant C/T snv 0.11 2
rs12408934
JAK1
1 64957764 intron variant G/A snv 6.1E-02 2
rs1754541
LOC101928334
1 101160327 intergenic variant A/G snv 0.25 2
rs2072735
SPSB1
1 9295413 intron variant A/C snv 0.76 2
rs2147904
HIVEP3
1 41905743 intron variant T/C snv 0.50 2
rs2296618
PTPRC
1 198697103 intron variant A/G snv 0.21 2
rs2502994
CNR2
1 23872873 3 prime UTR variant T/A;C snv 2
rs3218192
E2F2
1 23514878 intron variant G/T snv 0.40 2
rs34645101
LOC107985203 ; MCL1
1 150578448 synonymous variant T/C snv 9.0E-03 7.9E-03 2
rs35249183 1 12039288 upstream gene variant A/G snv 6.4E-02 2
rs41369048
HLX-AS1 ; HLX
1 220878224 intron variant A/G snv 9.7E-02 2
rs66538782
PIK3R3 ; P3R3URF-PIK3R3
1 46130565 intron variant A/-;AA;AAA delins 2
rs6684992 1 87286317 intergenic variant A/T snv 0.20 2
rs797680
CCDC18
1 93251417 intron variant G/A;T snv 2
rs945631
DIPK1A
1 92960610 intron variant G/A snv 4.1E-02 2
rs1004870
HIVEP3
1 41905116 intron variant C/T snv 0.57 1
rs1013910 1 116868761 intergenic variant G/A snv 0.91 1
rs1071849
UBXN11 ; CD52
1 26320235 missense variant A/G snv 0.67 0.70 1
rs10794666
LOC107984932 ; RUNX3
1 24924339 intron variant C/T snv 0.45 1
rs10864462
PEX14
1 10552101 intron variant A/T snv 0.11 1
rs1099448
TNFSF4 ; LOC100506023
1 173262759 intergenic variant C/T snv 0.58 1
rs11164971 1 91576688 regulatory region variant T/G snv 0.15 1
rs11264296
DCST2
1 155022274 intron variant T/C snv 0.45 1