Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 5
rs4601790
EHBP1L1
11 65586435 intron variant A/G snv 0.23 4
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 4
rs10504249
LINC01602 ; LOC105375856
8 57876522 intron variant A/G snv 1.7E-02 3
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 3
rs3792765
NPR3
5 32713730 intron variant A/G snv 0.36 2
rs7286472 22 33990484 intergenic variant A/G snv 0.19 2
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 4
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs1275986 2 26689211 upstream gene variant C/A snv 0.50 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs11953630 5 158418394 intergenic variant C/A;T snv 3