Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs2533291
PTPRN2
0.925 0.120 7 157712962 intron variant C/T snv 0.12 2
rs2944542
ZNF365
0.925 0.120 10 62610240 intron variant C/G snv 0.71 2
rs380743
RASIP1
0.925 0.120 19 48737757 intron variant G/A;C snv 2
rs3917265
IL1R1
1.000 0.120 2 102162001 intron variant T/C snv 0.50 2
rs4363385
LOC105371446
0.925 0.120 1 153016845 upstream gene variant T/C snv 0.62 2
rs45616239
KIAA1109
0.925 0.120 4 122335010 intron variant T/C snv 0.13 2
rs62176107
PRKRA ; CHROMR
0.925 0.120 2 178436244 missense variant G/A;T snv 2
rs6548123
MYT1L
0.925 0.120 2 2221629 intron variant C/T snv 0.76 2
rs6596086
RAD50
0.925 0.120 5 132616530 intron variant T/C snv 0.34 2
rs6684514
TMEM79 ; SMG5
0.925 0.120 1 156285665 missense variant G/A snv 0.27 0.24 2
rs67766926 0.925 0.120 2 60936446 downstream gene variant C/G snv 0.17 2
rs73510898
ZGLP1
0.925 0.120 19 10305768 intron variant G/A;C;T snv 2
rs80312298
MGMT
0.925 0.120 10 129683009 intron variant C/A;T snv 2
rs9302874 0.925 0.120 17 78284479 intergenic variant C/T snv 0.24 2
rs9405490
LOC102723944
0.925 0.120 6 1510423 downstream gene variant G/A snv 0.20 2
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs10199605
LINC00299
1.000 0.120 2 8354967 intron variant G/A snv 0.26 1
rs10214237 1.000 0.120 5 35883632 downstream gene variant T/C snv 0.21 1
rs10738626 1.000 0.120 9 22373458 intergenic variant C/G;T snv 1
rs10888499 1.000 0.120 1 152560266 intergenic variant C/A;T snv 1