Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5