Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001494
ST7L
1 112567997 intron variant T/C snv 0.50 1
rs10062757 5 62239297 intergenic variant T/C snv 0.35 1
rs10072221
IQGAP2
5 76424719 intron variant T/A;C;G snv 1
rs10076782
RNF145
5 159177955 intron variant G/A snv 0.41 1
rs10220411
ACTN1-AS1
14 68985371 intron variant A/G snv 0.29 2
rs10274553
CTB-30L5.1
7 106716200 intron variant T/A;C snv 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10506328
NFE2
12 54293448 intron variant A/C snv 0.75 1
rs10512627
KALRN
3 124621375 intron variant G/C snv 0.43 1
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs10605167
ENDOD1
11 95095304 intron variant TCC/-;TCCTCC delins 1
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs10813766
DOCK8
9 331490 intron variant T/G snv 0.64 1
rs10821556 9 134077014 upstream gene variant C/A snv 0.37 1
rs10876550
COPZ1
12 54318524 intron variant G/A snv 0.68 2
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs10900828 5 134500603 upstream gene variant T/A;C;G snv 1
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 2
rs10940072
MAST4
5 66620956 intron variant G/A snv 0.37 2
rs10954750
STYXL1
7 76035603 intron variant C/A;G snv 1
rs10990535
SLC35D2
9 96328727 intron variant C/T snv 0.27 1
rs11030122
STIM1
11 3865946 intron variant C/G snv 0.27 2
rs11043280
WDR66
12 121988737 intron variant T/C snv 0.32 1
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7