Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80133860
EPM2A
6 145673722 intron variant G/A;T snv 1
rs80012730 12 49277876 upstream gene variant A/C snv 6.1E-02 2
rs7973618
BAZ2A
12 56625659 intron variant T/C;G snv 1
rs7961894
WDR66
12 121927677 intron variant C/T snv 7.3E-02 2
rs7949566
ST3GAL4
11 126415406 intron variant G/A snv 0.45 2
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 4
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs7869524
DOCK8
9 341829 intron variant G/T snv 0.52 1
rs78363913
ASAP1
8 130167315 intron variant AA/-;A;AAA;AAAA delins 0.59 1
rs78346539
DNM3
1 171966088 intron variant C/G snv 8.6E-03 2
rs781329210 12 51279917 downstream gene variant TTTT/-;T;TT;TTT;TTTTT;TTTTTTT delins 9.5E-02 1
rs779314480 20 59010966 upstream gene variant TTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTTTTTTTTT delins 1
rs77795865
PEAR1
1 156908681 missense variant C/T snv 2.0E-02 2.3E-02 1
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs7743045
SELENOKP3
6 118781108 intron variant A/G snv 0.65 1
rs77327054
DCAF5
14 69129366 intron variant A/G snv 4.2E-02 1
rs7722711
IQGAP2
5 76611026 missense variant T/C snv 7.6E-02 5.5E-02 1
rs7712401
PPIC-AS1
5 123038764 intron variant C/T snv 0.58 1
rs76900683
LNX2
13 27583898 intron variant G/C snv 3.0E-02 2
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7641175
TBC1D5
3 18269920 intron variant G/A snv 0.81 3
rs7596219 2 66415818 intergenic variant A/G snv 0.14 1
rs7585866 2 191831529 downstream gene variant A/G snv 0.24 2
rs75763843
LINC01478
18 44482415 intron variant A/C;T snv 2
rs75446219
LDLRAP1
1 25551001 intron variant C/T snv 2.0E-02 1