Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1270901
SPATS2
12 49441462 intron variant G/A snv 0.97 1
rs11910328
LINC01700
21 38978818 upstream gene variant G/A snv 0.85 1
rs4811196
CTNNBL1
20 37841292 intron variant G/A snv 0.81 1
rs498079
EYA4
6 133241318 intron variant G/C snv 0.81 1
rs2531992
ADCY9
16 3971733 intron variant A/G snv 0.80 2
rs1021188 13 42541997 intergenic variant C/T snv 0.79 1
rs11898505
SPTBN1
2 54457420 intron variant A/G snv 0.76 1
rs10824760
LNCAROD ; LOC105378305
10 52665565 intron variant C/T snv 0.75 1
rs1373004
LNCAROD ; LOC105378305
10 52668065 intron variant T/G snv 0.75 1
rs2130604 6 126499415 intron variant T/G snv 0.75 1
rs6510186
TSHZ3
19 31163709 intron variant T/C snv 0.75 1
rs271170
LINC00326
6 132994665 intron variant T/C snv 0.74 1
rs2873195
SMG6
17 2161408 intron variant A/T snv 0.74 1
rs921874
FZD4-DT ; LOC105369422
11 87012962 intron variant A/C snv 0.74 1
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs7398996 12 53265664 upstream gene variant C/T snv 0.72 1
rs7781370
LOC105375411 ; SEM1
7 96504219 intron variant T/C snv 0.72 1
rs1159798
LNCAROD ; LOC105378305
10 52652733 intron variant A/C snv 0.70 1
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs2553773
LOC105376626
11 35062086 regulatory region variant C/G snv 0.69 1
rs273573
DCDC1 ; LOC105376611
11 30889444 intron variant A/C snv 0.69 1
rs10735851 12 53349280 upstream gene variant G/A snv 0.68 1
rs11934731 4 87910097 intergenic variant G/A snv 0.67 1
rs2062377
COLEC10
8 118995181 upstream gene variant T/A snv 0.67 1
rs3018362 0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67 2