Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 2
rs78154696 1.000 0.080 5 1000041 upstream gene variant G/A;T snv 1
rs9833888
CMSS1 ; FILIP1L
1.000 0.080 3 100004736 intron variant G/T snv 0.18 1
rs10988944
ERP44
0.925 0.040 9 100011933 intron variant C/A snv 0.20 2
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv 3
rs7323466 13 100019615 intergenic variant T/C snv 0.64 1
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4
rs56079856
IDUA
4 1000223 intron variant G/T snv 0.14 1
rs7826222 1.000 0.080 8 10002570 intron variant G/C snv 1
rs1963304
ZKSCAN1
7 100028173 intron variant T/A;G snv 1
rs1015538
ZKSCAN1
7 100028412 intron variant A/G snv 0.72 1
rs2897075
ZKSCAN1
1.000 0.040 7 100032719 intron variant C/T snv 0.31 1
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 2
rs9585327 1.000 0.040 13 100037100 intergenic variant G/A snv 0.36 1
rs181978376 10 100037758 downstream gene variant T/A;C snv 1
rs4486555 10 100039545 downstream gene variant G/T snv 0.40 1
rs66803065
SBF2
11 10004305 intron variant C/A;T snv 0.19 2
rs4295981
CPN1
10 100043668 intron variant C/T snv 0.37 1
rs11599750
CPN1
10 100045685 intron variant C/T snv 0.40 2
rs4919420
CPN1
10 100046495 intron variant A/G snv 0.40 1
rs13001130
AFF3
2 100052237 intron variant G/A snv 0.15 1
rs397807524
ADAMTS17
15 100052239 intron variant -/AA ins 7.0E-06 1
rs78633727
AFF3
2 100052995 intron variant T/C snv 0.16 1
rs6750720
AFF3
2 100054283 intron variant C/G;T snv 1
rs10209110
AFF3
1.000 0.120 2 100056230 intron variant C/T snv 0.47 1