Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10277664
TBXAS1
1.000 0.040 7 139806781 intron variant C/T snv 0.36 1
rs1033023 1.000 0.040 1 239045834 intergenic variant T/A snv 0.36 1
rs1033394
HDAC2-AS2 ; LOC107986638
1.000 0.040 6 114392159 intron variant C/T snv 0.77 1
rs1035578
SNX29
1.000 0.040 16 12437508 intron variant G/A snv 0.57 2
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 1
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs10425465
PEPD
1.000 0.040 19 33407028 intron variant T/G snv 0.34 1
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 2
rs1042992
BNIP3L
1.000 0.040 8 26411675 3 prime UTR variant C/T snv 0.19 1
rs10429924 1.000 0.040 1 244227262 intergenic variant C/T snv 8.8E-02 1
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 1
rs10489202
MPC2
0.925 0.080 1 167933841 intron variant G/T snv 0.20 2
rs10490175
NRXN1
1.000 0.040 2 50855616 intron variant G/A snv 0.16 2
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10503256
CSMD1
1.000 0.040 8 4356657 intron variant A/G snv 0.57 1
rs10509852 1.000 0.040 10 107815336 intron variant C/A;T snv 1
rs1051061
VRK2
1.000 0.040 2 58089679 missense variant A/G snv 0.36 0.31 1
rs10510653
OSBPL10
1.000 0.040 3 32017067 intron variant T/A snv 0.23 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs10520163
CLCN3
1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1064395
NCAN
0.882 0.120 19 19250926 3 prime UTR variant G/A snv 0.24 1