Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11216183
SIK3
11 116910829 intron variant C/A snv 0.10 3
rs11666808
IQCN
1.000 0.040 19 18272696 intron variant T/C snv 0.67 3
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 3
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 3
rs1250258
LOC105373868 ; FN1
1.000 0.040 2 215435462 intron variant C/T snv 0.79 3
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 3
rs1385167
LOC105369168
2 65973514 intron variant A/G snv 0.18 3
rs1534696
SNX10
7 26357619 intron variant C/A snv 0.58 3
rs1569135
LOC105373786
2 187250671 intron variant A/G snv 0.51 3
rs16996700
LINC01524 ; LOC105372666
20 52365406 intron variant T/C snv 0.29 3
rs1936805
RSPO3
6 127130971 intron variant C/T snv 0.55 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2047937
ZNF423
0.925 0.120 16 49830880 intron variant C/T snv 0.50 3
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 3
rs2276824
PBRM1
3 52603470 intron variant C/G snv 0.54 0.61 3
rs28451064 0.925 0.080 21 34221526 intron variant G/A snv 9.2E-02 3
rs34668726
KLHL29
1.000 0.040 2 23673031 intron variant C/G snv 0.13 3
rs3936510
C5orf67
1.000 0.040 5 56565039 intron variant G/A;T snv 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs4738141
EYA1
8 71557507 intron variant A/G snv 0.41 3
rs605066 6 139508529 intron variant C/T snv 0.53 3
rs61823192
LYPLAL1-DT
1 219121228 intron variant C/T snv 1.6E-02 3
rs634869 6 139510620 intron variant T/A;C snv 3
rs714515
DNM3 ; PIGC
1 172383850 intron variant G/A snv 0.46 3
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 3