Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 1
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 1
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 1
rs12902602
LOC112268142 ; CHRNB4
15 78675059 intron variant A/G snv 0.28 1
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs2836754
LOC400867
1.000 0.040 21 38919816 intron variant T/C snv 0.50 1
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 1
rs643507
LPIN2 ; CHORDC1P4
1.000 0.080 18 2946293 non coding transcript exon variant C/T snv 0.96 0.92 1
rs1514174
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74527379 intron variant C/T snv 0.44 1
rs11012732
MLLT10
0.882 0.080 10 21541175 intron variant A/G snv 0.31 1
rs7638110
MRPS22
1.000 0.080 3 139185143 intron variant G/T snv 9.4E-02 1
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 1
rs7574314
NBEAL1
2 203099414 intron variant T/C snv 0.41 1
rs3132947
NOTCH4
1.000 0.120 6 32209005 intron variant G/T snv 0.19 1
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 1
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21 1
rs2516739
NTHL1 ; TSC2
16 2047157 non coding transcript exon variant G/A snv 0.30 1
rs2590838
PBRM1
3 52588070 intron variant G/A snv 0.55 1
rs215607
PDE1C
7 32298725 missense variant G/A snv 0.79 0.77 1
rs215614
PDE1C
7 32307723 intron variant G/A snv 0.62 1
rs215634
PDE1C
7 32329536 intron variant A/G;T snv 1
rs7779181
PDE1C
7 32305671 intron variant T/C snv 0.22 1
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 1