Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs425277
PRKCZ
1 2137733 intron variant C/T snv 0.23 1
rs4601530 1 24717620 downstream gene variant C/T snv 0.31 1
rs6662509
H6PD
1 9257545 intron variant C/T snv 0.17 1
rs6684205
TGFB2
1 218436360 intron variant A/G;T snv 1
rs6686842
SCMH1
1 41065199 intron variant T/C snv 0.65 1
rs6699417
PKN2-AS1
1 88657760 intron variant C/T snv 0.61 1
rs678962
DNM3
1 172220749 intron variant T/G snv 0.24 1
rs7532866
LIN28A
1 26415053 intron variant A/G snv 0.36 1
rs7534091 1 118321993 intergenic variant A/G snv 0.23 1
rs7552186 1 218821931 intergenic variant C/T snv 0.40 1
rs9428104 1 118312964 intergenic variant A/G;T snv 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 2
rs6706968
LOC105373585
0.925 0.120 2 120552693 non coding transcript exon variant A/C;G snv 2
rs10187066
ZNF142
2 218650036 intron variant A/G snv 0.45 1
rs1052483 2 219069626 non coding transcript exon variant G/T snv 0.13 1
rs11684404
EIF2AK3
2 88625104 intron variant T/C snv 0.28 1
rs11895026
CENPO
2 24813989 intron variant C/A;T snv 1
rs12470505
CFAP65
2 219043647 upstream gene variant T/G snv 0.19 1
rs12474201 2 46694146 upstream gene variant G/A snv 0.30 1
rs12612930
ZNF638
2 71298655 intron variant T/C snv 4.5E-02 1
rs12694997
SEPTIN2
2 241323571 intron variant G/A snv 0.19 1
rs13428823
EFR3B
2 25150429 intron variant G/A snv 0.59 1