Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs708730
SLC41A1
1.000 0.040 1 205808652 intron variant G/A snv 0.66 1
rs417968
LINC02210 ; LINC02210-CRHR1
1.000 0.040 17 45651010 non coding transcript exon variant G/A snv 0.65 2
rs947211
LOC105371702
0.925 0.040 1 205783537 non coding transcript exon variant A/G snv 0.64 2
rs2862909
TPTE2P6 ; LOC105370117
1.000 0.040 13 24527029 intron variant G/T snv 0.63 1
rs7185232
RABEP2
1.000 0.040 16 28922147 intron variant C/T snv 0.62 1
rs6430538
CCNT2-AS1
0.925 0.080 2 134782397 intron variant C/T snv 0.62 1
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 2
rs482912
LAMP3
1.000 0.040 3 183135882 missense variant T/C snv 0.65 0.59 1
rs2666781
DNAJC1
1.000 0.040 10 21916747 intron variant C/A snv 0.58 1
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 2
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs1411478
STX6
0.925 0.120 1 180993146 intron variant A/G snv 0.56 1
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs1526123
LINC02210-CRHR1
1.000 0.040 17 45705974 intron variant T/C snv 0.55 1
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 1
rs356165
SNCA
0.882 0.080 4 89725735 3 prime UTR variant G/A snv 0.54 1
rs356203
SNCA
1.000 0.040 4 89744890 intron variant C/T snv 0.54 1
rs4925114
RAI1
0.925 0.080 17 17807956 intron variant A/G snv 0.53 1
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 1
rs132985
PLA2G6
0.827 0.120 22 38167464 intron variant C/T snv 0.51 1
rs1504212 1.000 0.040 5 53824125 upstream gene variant C/A snv 0.51 1
rs213462 1.000 0.040 X 83449447 intergenic variant A/C snv 0.50 1
rs7640612
MCCC1
1.000 0.040 3 183025479 intron variant C/A snv 0.50 1