Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2009733
KANK3
19 8333830 missense variant A/C;G snv 1.4E-05; 0.48 1
rs3934939
TMEM255B
13 113801017 intron variant A/C;G snv 1
rs772178
SNRNP200
2 96297946 intron variant A/C;G snv 1
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs10747570
COX14
12 50116154 intron variant A/C;G;T snv 2
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs9375463 6 126845743 intron variant A/C;T snv 3
rs351364
WNT2B
1 112502439 intron variant A/C;T snv 0.72 2
rs9286060 8 9795635 intergenic variant A/C;T snv 2
rs12938803
EPN2 ; EPN2-AS1
17 19301119 intron variant A/C;T snv 1
rs2541918 7 35435712 intergenic variant A/C;T snv 1
rs2978098
LOC105375672 ; SNX31
8 100664447 upstream gene variant A/C;T snv 1
rs55829085
POLN ; HAUS3
4 2163766 intron variant A/C;T snv 1
rs7020564
ZNF462
9 106907735 intron variant A/C;T snv 1
rs7431604
RYK
3 134172151 intron variant A/C;T snv 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 6