Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10031466
TRIML2
4 188094248 intron variant G/A snv 0.56 2
rs1003858
PAPPA
9 116202676 intron variant G/C snv 1.1E-02 2
rs10041657
FER
5 108816727 intron variant G/A snv 0.23 2
rs1014667
NRXN1
2 50521617 intron variant G/A;C snv 2
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs1021071
CHRNB4 ; LOC112268142
15 78675837 intron variant G/C snv 0.28 2
rs10236197
PDE1C
7 32252149 intron variant T/C snv 0.41 1
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3
rs10269774
CDK6
7 92624658 intron variant G/A snv 0.36 2
rs10425738
CYP2G1P
19 40911822 non coding transcript exon variant G/A snv 0.74 2
rs10440708 5 173223484 downstream gene variant A/G snv 4.3E-02 2
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs10488693
DAGLA
11 61717684 intron variant C/T snv 6.0E-02 2
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 2
rs10501157
TRAF6
11 36485319 3 prime UTR variant T/C snv 1.6E-02 2
rs10503023 18 59165543 intergenic variant G/A snv 0.21 2
rs10508503 1.000 0.080 10 16257952 intergenic variant C/A;T snv 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 2
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 1
rs10783615
HOXC12 ; LOC105369775
12 53955989 intron variant G/A snv 0.71 2
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 1
rs10842707 12 26318431 intron variant C/G;T snv 4