Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11 3
rs114948639
PRKCE
2 46066687 intron variant C/T snv 7.2E-03 3
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs11689538
TFCP2L1
2 121238062 intron variant G/C snv 0.11 3
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 3
rs12811512
GPRC5A
12 12893277 intron variant C/T snv 0.11 3
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 3
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 3
rs149804345 3 56710234 intergenic variant AACAAA/-;AACAAAAACAAA;AACAAAAACAAAAACAAA delins 3
rs17287978 6 43973400 intergenic variant T/C snv 3.3E-02 3
rs17773190
LINC01118
2 46803224 intron variant A/G snv 0.32 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs218264 4 54542708 intergenic variant A/G;T snv 3
rs2236496
RCL1
9 4844265 intron variant T/C snv 0.19 3
rs2269188
SIM2 ; LOC107985492 ; LOC105369308
21 36700056 intron variant G/C snv 0.24 3
rs2279434
MARCHF8
10 45459616 intron variant C/T snv 7.1E-02 3
rs2732480
ZNF641
12 48342520 3 prime UTR variant C/A snv 0.39 3
rs2871993 19 35456988 intergenic variant G/A snv 0.25 3
rs35060063 3 194956076 intergenic variant G/A snv 0.36 3
rs35542019
LINC00649 ; LOC101928126
21 33974555 non coding transcript exon variant AA/-;A delins 0.57 3
rs366684
PROX1
1 214013919 intron variant G/A;C snv 3
rs3847858 12 51924594 downstream gene variant A/T snv 8.9E-02 3
rs4760682
PFKM
12 48118502 missense variant C/A snv 0.85 0.87 3
rs4823308
LINC01589
22 45604058 downstream gene variant T/A snv 0.38 3