Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 3
rs2871960
ZBTB38
3 141402972 5 prime UTR variant A/C snv 0.55 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs10152591
DRAIC ; LOC107984788
15 69755818 intron variant A/C snv 9.8E-02 1
rs10770705
SLCO1C1
12 20704533 intron variant A/C snv 0.70 1
rs10799445 1 227724182 upstream gene variant A/C snv 0.27 1
rs12298541
HMGA2
12 65912661 intron variant A/C snv 0.68 1
rs13210323
ANKS1A
6 35037307 intron variant A/C snv 0.30 1
rs2074974
DCAF16 ; NCAPG
4 17810992 5 prime UTR variant A/C snv 0.71 1
rs3103267
DIS3L2
2 232123872 intron variant A/C snv 0.72 1
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 1
rs6180
GHR
0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 1
rs6473015 8 77266249 intergenic variant A/C snv 0.23 1
rs7153027 14 91960878 intergenic variant A/C snv 0.44 1
rs910316
TMED10
14 75159339 intron variant A/C snv 0.45 1
rs9969804
IPPK
9 92666838 intron variant A/C snv 0.68 1
rs17818399
PIGF
2 46598887 intron variant A/C;G snv 1
rs2941551 17 63901188 upstream gene variant A/C;G snv 1
rs4338381
COL11A1
1.000 0.040 1 103107371 intron variant A/C;G snv 1
rs4752805
PTPRJ
11 47996803 intron variant A/C;G snv 1
rs4794665 1.000 0.160 17 56772968 intergenic variant A/C;G snv 1
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 1
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs8099594 1.000 0.040 18 49464790 upstream gene variant A/C;G;T snv 1