Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10842994
LOC105369709
1.000 0.080 12 27812217 intergenic variant C/T snv 0.15 1
rs10882095
KIF11
1.000 0.080 10 92634645 intron variant T/G snv 0.30 1
rs10882102 1.000 0.080 10 92706738 downstream gene variant G/A;C snv 1
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 1
rs10886471
GRK5
1.000 0.080 10 119389891 intron variant C/T snv 0.39 1
rs10906111 1.000 0.080 10 12260358 intergenic variant C/A;G;T snv 1
rs10906115 1.000 0.080 10 12272998 intergenic variant A/G snv 0.37 1
rs10908278
HNF1B
0.925 0.160 17 37739961 intron variant A/C;T snv 1
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 2
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs10946403
CDKAL1
1.000 0.080 6 20717173 intron variant A/G snv 0.30 1
rs10946406
LOC107986577 ; CDKAL1
1.000 0.080 6 20758529 intron variant A/G;T snv 1
rs10965243 1.000 0.080 9 22130066 downstream gene variant A/G snv 0.13 1
rs10965250 1.000 0.080 9 22133285 intergenic variant G/A snv 0.14 1
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3
rs11036627 1.000 0.080 11 41903164 intergenic variant C/A;T snv 1
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 1
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 2
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs11107116
SOCS2
1.000 0.080 12 93584728 downstream gene variant G/A;T snv 1