Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs295259
RCL1
1.000 0.040 9 4844507 intron variant G/A;C;T snv 0.90 1
rs4546904
PTGFRN
1 116945089 missense variant T/A snv 0.89; 2.8E-05; 8.1E-06 0.87 1
rs7524755
TMCO1
1.000 0.040 1 165725660 3 prime UTR variant T/A;C snv 0.89 1
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs6297
LOC105377864 ; HTR1B
6 77462224 3 prime UTR variant C/A;T snv 0.89 1
rs757123
MSI1
1.000 0.120 12 120363020 intron variant A/G snv 0.89 0.88 1
rs10739700
ST6GALNAC4
9 127909942 intron variant C/A;T snv 2.4E-05; 0.89 1
rs2228445
ATP2B4
1 203698281 synonymous variant T/A;C snv 0.89 1
rs6537825
TRIM33
1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 1
rs9938751
SHISA9
1.000 0.200 16 12908502 missense variant T/A;C snv 0.88 1
rs4242182
MSX2
5 174729165 missense variant T/A;C;G snv 4.0E-06; 0.88; 1.2E-05 1
rs26008
FNIP1
5 131672501 missense variant T/A;C snv 0.88 1
rs217116
CTSC
11 88300493 intron variant A/C;G;T snv 0.88; 8.0E-06 1
rs1419114
ATP2B4
1 203683316 synonymous variant A/G snv 0.88 0.83 2
rs3747869
VSIR ; CDH23
10 71760875 missense variant A/C snv 0.88 0.90 1
rs6436672
COL4A3 ; MFF-DT
1.000 0.040 2 227284391 non coding transcript exon variant A/G;T snv 0.88 1
rs7406910
HOXB7
17 48610894 missense variant T/C snv 0.88 0.88 3
rs5757973
IGLV1-47
22 22358119 missense variant T/A;C;G snv 1.2E-05; 0.88 1
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs2250889
SLC12A5-AS1 ; MMP9
0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 1
rs10412087
ZNF555
1.000 0.040 19 2853568 missense variant A/C;G snv 0.88 1
rs646356
MROH7-TTC4 ; MROH7
1.000 0.080 1 54702100 missense variant T/A snv 0.87 0.89 1
rs762679
MCM4
8 47972876 missense variant T/A snv 0.87 0.88 4
rs1654425
GP6 ; LOC107985325
19 55027612 synonymous variant T/C;G snv 0.87; 4.0E-05 1
rs784507
TTC21A
1.000 0.040 3 39125018 intron variant A/G snv 0.87 0.82 1