Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 5
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5