Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19 10
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18 10
rs704017
ZMIZ1-AS1
0.776 0.080 10 79059375 intron variant A/G snv 0.55 10
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv 9
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 9
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs76316943
UTP23
0.790 0.080 8 116836068 intron variant G/A snv 1.3E-02 9
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs12144319
TTC22
0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 10
rs12143541
TTC22
0.790 0.080 1 54782179 intron variant A/G snv 0.11 9
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs6031311
TOX2
0.776 0.080 20 44037835 intron variant C/T snv 0.73 10
rs3801081
TNS3
0.790 0.080 7 47471563 intron variant A/G snv 0.68 9
rs2052678
TMTC1
0.790 0.080 12 29680396 intron variant G/A snv 0.21 10
rs1963413
TMEM91 ; B9D2
0.776 0.080 19 41365668 intron variant G/A;C;T snv 10
rs9797885
TMEM91
0.790 0.080 19 41367096 intron variant A/G;T snv 9
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 9
rs4711689
TFEB
0.790 0.080 6 41725074 intron variant G/A;C snv 9