Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 2
rs11655198
ZPBP2
1.000 0.080 17 39869916 intron variant C/T snv 0.43 1
rs112502960
ZNF652 ; LOC102724596
1.000 0.080 17 49361940 5 prime UTR variant G/A snv 0.28 1
rs2288884
ZNF614 ; LOC112268244
1.000 0.080 19 52029018 intron variant C/T snv 0.14 1
rs12460587
ZNF432 ; ZNF841
1.000 0.080 19 52083666 intron variant T/C;G snv 0.16 1
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs114357009
ZNF311
1.000 0.080 6 28997735 intron variant G/A snv 3.2E-02 1
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 1
rs12447718
ZFPM1
1.000 0.080 16 88503726 intron variant G/A snv 8.4E-02 1
rs2315646
ZBTB46
1.000 0.080 20 63748397 intron variant T/A;G snv 1
rs3741578
ZBTB39
1.000 0.080 12 57000851 3 prime UTR variant G/C snv 6.8E-02 1
rs7625643
ZBTB38
0.925 0.080 3 141431184 intron variant A/G snv 0.51 3
rs1672691
ZBTB16
1.000 0.080 11 114071429 intron variant C/T snv 0.19 1
rs6982751
XKR6
0.925 0.120 8 10955964 intron variant C/G;T snv 2
rs2416257
WDR36
0.882 0.160 5 111099792 intron variant C/G;T snv 1
rs6736411
WDPCP
0.925 0.120 2 63446926 intron variant G/A snv 0.78 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs7521681
VAV3
0.925 0.120 1 107779913 intron variant G/A snv 0.15 2
rs7169793
UNC13C
1.000 0.080 15 53872840 intergenic variant G/C snv 0.93 1
rs7864027
UHRF2
1.000 0.080 9 6504189 intron variant A/C;T snv 1
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs1887704
UBAC2
0.925 0.080 13 99322238 intron variant C/G snv 0.55 2
rs59186511
UBAC2
1.000 0.080 13 99333984 intron variant C/T snv 0.13 1
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2